11-8132510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132510
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132510
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.1058C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.602C>T
  hgvsp: ENSP00000395320.2:p.Pro201Leu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.929C>T
  hgvsp: ENSP00000431658.1:p.Pro310Leu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*762C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.698C>T
  hgvsp: ENSP00000443871.1:p.Pro233Leu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.359C>T
  hgvsp: ENSP00000379910.2:p.Pro120Leu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.845C>T
  hgvsp: ENSP00000308820.6:p.Pro282Leu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.842C>T
  hgvsp: ENSP00000344904.4:p.Pro281Leu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.703C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*307C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.299C>T
  hgvsp: ENSP00000333988.7:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro282Leu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-8132533-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132533
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132533
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.336T>C
  hgvsp: ENST00000396677.2:c.336T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*284T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.822T>C
  hgvsp: ENST00000309737.6:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.579T>C
  hgvsp: ENST00000425599.2:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.819T>C
  hgvsp: ENST00000343202.4:c.819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.680T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.276T>C
  hgvsp: ENST00000335425.7:c.276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.906T>C
  hgvsp: ENST00000531450.1:c.906T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*739T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.1035T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.675T>C
  hgvsp: ENST00000539720.1:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp274Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

11-8132541-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132541
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132541
    reference: chr 11
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.814G>C
  hgvsp: ENSP00000308820.6:p.Glu272Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.898G>C
  hgvsp: ENSP00000431658.1:p.Glu300Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.672G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*731G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.571G>C
  hgvsp: ENSP00000395320.2:p.Glu191Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.268G>C
  hgvsp: ENSP00000333988.7:p.Glu90Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*276G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.328G>C
  hgvsp: ENSP00000379910.2:p.Glu110Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.667G>C
  hgvsp: ENSP00000443871.1:p.Glu223Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.811G>C
  hgvsp: ENSP00000344904.4:p.Glu271Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.1027G>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu272Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

11-8132542-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132542
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132542
    reference: chr 11
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.267A>G
  hgvsp: ENST00000335425.7:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.1026A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.897A>G
  hgvsp: ENST00000531450.1:c.897A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.671A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*275A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*730A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.327A>G
  hgvsp: ENST00000396677.2:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.810A>G
  hgvsp: ENST00000343202.4:c.810A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.666A>G
  hgvsp: ENST00000539720.1:c.666A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.813A>G
  hgvsp: ENST00000309737.6:c.813A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.570A>G
  hgvsp: ENST00000425599.2:c.570A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu271Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-8132559-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132559
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132559
    reference: chr 11
allele count: 28
allele frequency: 2.306349049454713e-4
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.250G>A
  hgvsp: ENSP00000333988.7:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.649G>A
  hgvsp: ENSP00000443871.1:p.Gly217Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.793G>A
  hgvsp: ENSP00000344904.4:p.Gly265Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.654G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*258G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.880G>A
  hgvsp: ENSP00000431658.1:p.Gly294Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.310G>A
  hgvsp: ENSP00000379910.2:p.Gly104Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.796G>A
  hgvsp: ENSP00000308820.6:p.Gly266Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.553G>A
  hgvsp: ENSP00000395320.2:p.Gly185Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*713G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.1009G>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly266Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

11-8132572-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132572
    reference: chr 11
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.867A>T
  hgvsp: ENST00000531450.1:c.867A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.783A>T
  hgvsp: ENST00000309737.6:c.783A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.780A>T
  hgvsp: ENST00000343202.4:c.780A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.636A>T
  hgvsp: ENST00000539720.1:c.636A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.297A>T
  hgvsp: ENST00000396677.2:c.297A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.540A>T
  hgvsp: ENST00000425599.2:c.540A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.996A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*245A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.641A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*700A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.237A>T
  hgvsp: ENST00000335425.7:c.237A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile261Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-8132583-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132583
    reference: chr 11
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.529G>T
  hgvsp: ENSP00000395320.2:p.Ala177Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.985G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.286G>T
  hgvsp: ENSP00000379910.2:p.Ala96Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.625G>T
  hgvsp: ENSP00000443871.1:p.Ala209Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*689G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.856G>T
  hgvsp: ENSP00000431658.1:p.Ala286Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*234G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.772G>T
  hgvsp: ENSP00000308820.6:p.Ala258Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.769G>T
  hgvsp: ENSP00000344904.4:p.Ala257Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.226G>T
  hgvsp: ENSP00000333988.7:p.Ala76Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.630G>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala258Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-8132588-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132588
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132588
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*229T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.524T>G
  hgvsp: ENSP00000395320.2:p.Leu175Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.620T>G
  hgvsp: ENSP00000443871.1:p.Leu207Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.851T>G
  hgvsp: ENSP00000431658.1:p.Leu284Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.764T>G
  hgvsp: ENSP00000344904.4:p.Leu255Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.980T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.625T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*684T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.767T>G
  hgvsp: ENSP00000308820.6:p.Leu256Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.281T>G
  hgvsp: ENSP00000379910.2:p.Leu94Arg
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.221T>G
  hgvsp: ENSP00000333988.7:p.Leu74Arg
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu256Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-8132592-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132592
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132592
    reference: chr 11
allele count: 3
allele frequency: 2.471495419495156e-5
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.616G>T
  hgvsp: ENSP00000443871.1:p.Glu206Ter
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*680G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.763G>T
  hgvsp: ENSP00000308820.6:p.Glu255Ter
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.520G>T
  hgvsp: ENSP00000395320.2:p.Glu174Ter
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.277G>T
  hgvsp: ENSP00000379910.2:p.Glu93Ter
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.847G>T
  hgvsp: ENSP00000431658.1:p.Glu283Ter
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.976G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.760G>T
  hgvsp: ENSP00000344904.4:p.Glu254Ter
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.621G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*225G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.217G>T
  hgvsp: ENSP00000333988.7:p.Glu73Ter
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu255Ter
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum

11-8132595-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132595
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132595
    reference: chr 11
allele count: 5
allele frequency: 4.119498409873614e-5
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.973A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.844A>G
  hgvsp: ENSP00000431658.1:p.Lys282Glu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.613A>G
  hgvsp: ENSP00000443871.1:p.Lys205Glu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.517A>G
  hgvsp: ENSP00000395320.2:p.Lys173Glu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*222A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.757A>G
  hgvsp: ENSP00000344904.4:p.Lys253Glu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.274A>G
  hgvsp: ENSP00000379910.2:p.Lys92Glu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.760A>G
  hgvsp: ENSP00000308820.6:p.Lys254Glu
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*677A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.618A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.214A>G
  hgvsp: ENSP00000333988.7:p.Lys72Glu
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys254Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

11-8132596-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132596
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132596
    reference: chr 11
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.756A>G
  hgvsp: ENST00000343202.4:c.756A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.213A>G
  hgvsp: ENST00000335425.7:c.213A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.273A>G
  hgvsp: ENST00000396677.2:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.617A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*676A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*221A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.972A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.759A>G
  hgvsp: ENST00000309737.6:c.759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.843A>G
  hgvsp: ENST00000531450.1:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.612A>G
  hgvsp: ENST00000539720.1:c.612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.516A>G
  hgvsp: ENST00000425599.2:c.516A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro253Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

11-8132598-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132598
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132598
    reference: chr 11
allele count: 22
allele frequency: 1.812728651000297e-4
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*674C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.271C>G
  hgvsp: ENSP00000379910.2:p.Pro91Ala
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.610C>G
  hgvsp: ENSP00000443871.1:p.Pro204Ala
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.514C>G
  hgvsp: ENSP00000395320.2:p.Pro172Ala
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.754C>G
  hgvsp: ENSP00000344904.4:p.Pro252Ala
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.970C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.757C>G
  hgvsp: ENSP00000308820.6:p.Pro253Ala
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.841C>G
  hgvsp: ENSP00000431658.1:p.Pro281Ala
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.615C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*219C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.211C>G
  hgvsp: ENSP00000333988.7:p.Pro71Ala
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro253Ala
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-8132609-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132609
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132609
    reference: chr 11
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*208A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*663A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.746A>G
  hgvsp: ENSP00000308820.6:p.Asp249Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.959A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.743A>G
  hgvsp: ENSP00000344904.4:p.Asp248Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.200A>G
  hgvsp: ENSP00000333988.7:p.Asp67Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.830A>G
  hgvsp: ENSP00000431658.1:p.Asp277Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.503A>G
  hgvsp: ENSP00000395320.2:p.Asp168Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.260A>G
  hgvsp: ENSP00000379910.2:p.Asp87Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.604A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.599A>G
  hgvsp: ENSP00000443871.1:p.Asp200Gly
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp249Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-8132610-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132610
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132610
    reference: chr 11
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.829G>T
  hgvsp: ENSP00000431658.1:p.Asp277Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.745G>T
  hgvsp: ENSP00000308820.6:p.Asp249Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.598G>T
  hgvsp: ENSP00000443871.1:p.Asp200Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.603G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.742G>T
  hgvsp: ENSP00000344904.4:p.Asp248Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*207G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.259G>T
  hgvsp: ENSP00000379910.2:p.Asp87Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.502G>T
  hgvsp: ENSP00000395320.2:p.Asp168Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.958G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.199G>T
  hgvsp: ENSP00000333988.7:p.Asp67Tyr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*662G>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp249Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-8132618-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132618
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132618
    reference: chr 11
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.590T>C
  hgvsp: ENSP00000443871.1:p.Ile197Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.595T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.734T>C
  hgvsp: ENSP00000344904.4:p.Ile245Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.950T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*654T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.251T>C
  hgvsp: ENSP00000379910.2:p.Ile84Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.737T>C
  hgvsp: ENSP00000308820.6:p.Ile246Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.494T>C
  hgvsp: ENSP00000395320.2:p.Ile165Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.821T>C
  hgvsp: ENSP00000431658.1:p.Ile274Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.191T>C
  hgvsp: ENSP00000333988.7:p.Ile64Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*199T>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile246Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-8132625-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132625
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132625
    reference: chr 11
allele count: 2
allele frequency: 1.657110661849998e-5
allele num: 120692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.487G>C
  hgvsp: ENSP00000395320.2:p.Glu163Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.727G>C
  hgvsp: ENSP00000344904.4:p.Glu243Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.814G>C
  hgvsp: ENSP00000431658.1:p.Glu272Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.583G>C
  hgvsp: ENSP00000443871.1:p.Glu195Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.588G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.730G>C
  hgvsp: ENSP00000308820.6:p.Glu244Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.184G>C
  hgvsp: ENSP00000333988.7:p.Glu62Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*192G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.244G>C
  hgvsp: ENSP00000379910.2:p.Glu82Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*647G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.943G>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu244Gln
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: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

11-8132631-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132631
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132631
    reference: chr 11
allele count: 1
allele frequency: 8.301235223801302e-6
allele num: 120464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.577A>G
  hgvsp: ENSP00000443871.1:p.Arg193Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.808A>G
  hgvsp: ENSP00000431658.1:p.Arg270Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.238A>G
  hgvsp: ENSP00000379910.2:p.Arg80Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*641A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.481A>G
  hgvsp: ENSP00000395320.2:p.Arg161Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.178A>G
  hgvsp: ENSP00000333988.7:p.Arg60Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.721A>G
  hgvsp: ENSP00000344904.4:p.Arg241Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.582A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.724A>G
  hgvsp: ENSP00000308820.6:p.Arg242Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.937A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*186A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg242Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

11-8132633-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132633
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132633
    reference: chr 11
allele count: 11
allele frequency: 9.132875029059147e-5
allele num: 120444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*184G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.935G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.806G>A
  hgvsp: ENSP00000431658.1:p.Arg269His
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*639G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.575G>A
  hgvsp: ENSP00000443871.1:p.Arg192His
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.719G>A
  hgvsp: ENSP00000344904.4:p.Arg240His
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.479G>A
  hgvsp: ENSP00000395320.2:p.Arg160His
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.236G>A
  hgvsp: ENSP00000379910.2:p.Arg79His
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.580G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.722G>A
  hgvsp: ENSP00000308820.6:p.Arg241His
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.176G>A
  hgvsp: ENSP00000333988.7:p.Arg59His
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16052
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19365
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg241His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

11-8132634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132634
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132634
    reference: chr 11
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*638C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.574C>T
  hgvsp: ENSP00000443871.1:p.Arg192Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.579C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.934C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.805C>T
  hgvsp: ENSP00000431658.1:p.Arg269Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.235C>T
  hgvsp: ENSP00000379910.2:p.Arg79Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.478C>T
  hgvsp: ENSP00000395320.2:p.Arg160Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.175C>T
  hgvsp: ENSP00000333988.7:p.Arg59Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.718C>T
  hgvsp: ENSP00000344904.4:p.Arg240Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*183C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.721C>T
  hgvsp: ENSP00000308820.6:p.Arg241Cys
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg241Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

11-8132636-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132636
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132636
    reference: chr 11
allele count: 1
allele frequency: 8.314348903337379e-6
allele num: 120274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.476A>C
  hgvsp: ENSP00000395320.2:p.Lys159Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.233A>C
  hgvsp: ENSP00000379910.2:p.Lys78Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.932A>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.716A>C
  hgvsp: ENSP00000344904.4:p.Lys239Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.572A>C
  hgvsp: ENSP00000443871.1:p.Lys191Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.803A>C
  hgvsp: ENSP00000431658.1:p.Lys268Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.173A>C
  hgvsp: ENSP00000333988.7:p.Lys58Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*636A>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.719A>C
  hgvsp: ENSP00000308820.6:p.Lys240Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*181A>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.577A>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys240Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

11-8132642-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132642
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132642
    reference: chr 11
allele count: 1
allele frequency: 8.346130733791815e-6
allele num: 119816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.926G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*175G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.167G>C
  hgvsp: ENSP00000333988.7:p.Cys56Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.566G>C
  hgvsp: ENSP00000443871.1:p.Cys189Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.797G>C
  hgvsp: ENSP00000431658.1:p.Cys266Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.713G>C
  hgvsp: ENSP00000308820.6:p.Cys238Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.710G>C
  hgvsp: ENSP00000344904.4:p.Cys237Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*630G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.470G>C
  hgvsp: ENSP00000395320.2:p.Cys157Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.571G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.227G>C
  hgvsp: ENSP00000379910.2:p.Cys76Ser
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11008
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys238Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-8132643-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132643
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132643
    reference: chr 11
allele count: 3
allele frequency: 2.504633572108401e-5
allele num: 119778
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.712T>G
  hgvsp: ENSP00000308820.6:p.Cys238Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.796T>G
  hgvsp: ENSP00000431658.1:p.Cys266Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*629T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.226T>G
  hgvsp: ENSP00000379910.2:p.Cys76Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.925T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.469T>G
  hgvsp: ENSP00000395320.2:p.Cys157Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.565T>G
  hgvsp: ENSP00000443871.1:p.Cys189Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*174T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.709T>G
  hgvsp: ENSP00000344904.4:p.Cys237Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.166T>G
  hgvsp: ENSP00000333988.7:p.Cys56Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.570T>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys238Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-8132649-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132649
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132649
    reference: chr 11
allele count: 1
allele frequency: 8.382651264942076e-6
allele num: 119294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.220T>A
  hgvsp: ENSP00000379910.2:p.Ser74Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*623T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.703T>A
  hgvsp: ENSP00000344904.4:p.Ser235Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.559T>A
  hgvsp: ENSP00000443871.1:p.Ser187Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.919T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.463T>A
  hgvsp: ENSP00000395320.2:p.Ser155Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.160T>A
  hgvsp: ENSP00000333988.7:p.Ser54Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*168T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.564T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.790T>A
  hgvsp: ENSP00000431658.1:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.706T>A
  hgvsp: ENSP00000308820.6:p.Ser236Thr
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser236Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

11-8132657-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132657
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132657
    reference: chr 11
allele count: 1
allele frequency: 8.423606314335294e-6
allele num: 118714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.455A>G
  hgvsp: ENSP00000395320.2:p.Tyr152Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.782A>G
  hgvsp: ENSP00000431658.1:p.Tyr261Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.152A>G
  hgvsp: ENSP00000333988.7:p.Tyr51Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.695A>G
  hgvsp: ENSP00000344904.4:p.Tyr232Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.212A>G
  hgvsp: ENSP00000379910.2:p.Tyr71Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*615A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.698A>G
  hgvsp: ENSP00000308820.6:p.Tyr233Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.551A>G
  hgvsp: ENSP00000443871.1:p.Tyr184Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.911A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*160A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.556A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr233Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

11-8132668-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132668
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132668
    reference: chr 11
allele count: 1
allele frequency: 8.494011721736177e-6
allele num: 117730
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.687T>C
  hgvsp: ENST00000309737.6:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.684T>C
  hgvsp: ENST00000343202.4:c.684T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.545T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.201T>C
  hgvsp: ENST00000396677.2:c.201T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.444T>C
  hgvsp: ENST00000425599.2:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.540T>C
  hgvsp: ENST00000539720.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*149T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.771T>C
  hgvsp: ENST00000531450.1:c.771T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.900T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.141T>C
  hgvsp: ENST00000335425.7:c.141T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*604T>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr229Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

11-8132676-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132676
    reference: chr 11
allele count: 1
allele frequency: 8.554905382746468e-6
allele num: 116892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.133G>C
  hgvsp: ENSP00000333988.7:p.Glu45Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.676G>C
  hgvsp: ENSP00000344904.4:p.Glu226Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.436G>C
  hgvsp: ENSP00000395320.2:p.Glu146Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.537G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.193G>C
  hgvsp: ENSP00000379910.2:p.Glu65Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.679G>C
  hgvsp: ENSP00000308820.6:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.763G>C
  hgvsp: ENSP00000431658.1:p.Glu255Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*596G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.892G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.532G>C
  hgvsp: ENSP00000443871.1:p.Glu178Gln
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*141G>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu227Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-8132683-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132683
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132683
    reference: chr 11
allele count: 1
allele frequency: 8.620541025154739e-6
allele num: 116002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.756T>C
  hgvsp: ENST00000531450.1:c.756T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.530T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.885T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*134T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.126T>C
  hgvsp: ENST00000335425.7:c.126T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.672T>C
  hgvsp: ENST00000309737.6:c.672T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.186T>C
  hgvsp: ENST00000396677.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*589T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.525T>C
  hgvsp: ENST00000539720.1:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.429T>C
  hgvsp: ENST00000425599.2:c.429T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.669T>C
  hgvsp: ENST00000343202.4:c.669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.672T>C
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-8132688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132688
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132688
    reference: chr 11
allele count: 2
allele frequency: 1.733132289987695e-5
allele num: 115398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-4C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-4C>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.671-4C>T
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: G
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-8132692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132692
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132692
    reference: chr 11
allele count: 35
allele frequency: 3.062385160556479e-4
allele num: 114290
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-8C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-8C>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17995
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.671-8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-8132702-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132702
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132702
    reference: chr 11
allele count: 1
allele frequency: 9.148293843198244e-6
allele num: 109310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-18T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-18T>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13451
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

11-8132704-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132704
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132704
    reference: chr 11
allele count: 1
allele frequency: 9.1568383268625e-6
allele num: 109208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-20T>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-20T>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9849
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-8132704-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132704
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132704
    reference: chr 11
allele count: 4
allele frequency: 3.662735330745e-5
allele num: 109208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-20T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-20T>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-8132721-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132721
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132721
    reference: chr 11
allele count: 1
allele frequency: 1.655355073663301e-5
allele num: 60410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-37C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-37C>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-8132721-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132721
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132721
    reference: chr 11
allele count: 2
allele frequency: 3.310710147326601e-5
allele num: 60410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-37C>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-37C>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13173
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22640
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

11-8132727-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132727
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
allele count: 3
allele frequency: 1.490016886858051e-4
allele num: 20134
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-44_884-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-44_668-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-44_529-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-44_428-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-44_755-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-44_*588-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-44_524-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-44_125-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-44_185-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-44_*133-43insT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-44_671-43insT
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14606
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-8132727-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132727
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132726
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 20134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-44delG
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-44delG
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: TC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-8132728-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132729
    reference: chr 11
allele count: 1380
allele frequency: 3.53556056568969e-2
allele num: 39032
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-45dupT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-45dupT
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 7.5e0
  variant carriers: 503
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.75e1
  variant carriers: 480
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 1.25e1
  variant carriers: 592
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.25e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 8.75e1
  variant carriers: 50
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/11-8132728-C-CAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132730
    reference: chr 11
allele count: 38
allele frequency: 9.735601557696249e-4
allele num: 39032
alternate allele: CAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-46_*588-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-46_125-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-46_185-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-46_671-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-46_668-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-46_529-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-46_755-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-46_*133-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-46_428-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-46_884-45dupTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-46_524-45dupTT
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22765
  bin: 2.5e0
  variant carriers: 4
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-8132728-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132727
    reference: chr 11
allele count: 17687
allele frequency: 4.53141012502562e-1
allele num: 39032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-45delT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-45delT
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 7.5e0
  variant carriers: 6954
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 530
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.25e1
  variant carriers: 2047
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.75e1
  variant carriers: 5282
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 1.25e1
  variant carriers: 9890
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 879
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 1215
num of homozygotes: 485
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: CA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/11-8132728-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132726
    reference: chr 11
allele count: 785
allele frequency: 2.011170321787251e-2
allele num: 39032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-46_185-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-46_*133-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-46_529-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-46_884-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-46_755-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-46_125-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-46_668-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-46_671-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-46_*588-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-46_524-45delTT
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-46_428-45delTT
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 1.25e1
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.75e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 7.5e0
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.25e1
  variant carriers: 135
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 5.75e1
  variant carriers: 43
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: CAA
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-8132728-CAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132725
    reference: chr 11
allele count: 17
allele frequency: 4.355400696864111e-4
allele num: 39032
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6474
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22765
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 1
  allele frequency: 2.845759817871372e-4
  allele num: 3514
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2992
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 1
  allele frequency: 3.012048192771084e-3
  allele num: 332
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 12
  allele frequency: 5.13083632632119e-4
  allele num: 23388
  num of homozygotes: 0
population: East Asian
population: South Asian
population: African
reference allele: CAAA
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-8132728-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132728
    reference: chr 11
allele count: 38
allele frequency: 9.735601557696249e-4
allele num: 39032
alternate allele: A
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18992
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 6474
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22765
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 2
  allele frequency: 6.684491978609625e-4
  allele num: 2992
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 332
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 4
  allele frequency: 1.524390243902439e-3
  allele num: 2624
  num of homozygotes: 0
population: African
  type: Population
  allele count: 3
  allele frequency: 8.426966292134832e-4
  allele num: 3560
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-8132733-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132733
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132733
    reference: chr 11
allele count: 1
allele frequency: 1.037452017844175e-5
allele num: 96390
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-49T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-49T>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15408
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7961
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-8132735-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8132735
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8132735
    reference: chr 11
allele count: 854
allele frequency: 8.84570765661253e-3
allele num: 96544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.185-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.755-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.529-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.884-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.428-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.668-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.524-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.671-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*588-51T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*133-51T>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13540
  bin: 1.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10039
  bin: 2.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 7.5e0
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 2.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 15333
  bin: 1.75e1
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 14
num of homozygotes: 43
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

11-8148158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148158
    reference: chr 11
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.523+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*132+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.184+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.528+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.670+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.667+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*587+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11661A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.883+48A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15474A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.754+48A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28513
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

11-8148165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148165
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148165
    reference: chr 11
allele count: 1548
allele frequency: 1.281414522697924e-2
allele num: 120804
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.883+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.523+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11654A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*587+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*132+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.667+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.754+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.528+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.184+41A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15481A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.670+41A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 28709
  bin: 2.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 3.25e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 2.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.25e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 3.75e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 47
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-8148173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148173
    reference: chr 11
allele count: 5
allele frequency: 4.135512472705618e-5
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.523+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.528+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*587+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*132+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.754+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.184+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11646G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15489G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.667+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.670+33G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.883+33G>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8315
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

11-8148198-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148198
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148198
    reference: chr 11
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*132+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.184+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.523+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.528+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*587+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.670+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.667+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15514G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11621G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.883+8G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.754+8G>C
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.670+8G>C
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-8148202-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148202
    reference: chr 11
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.667+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.523+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.670+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.184+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.754+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15518A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.883+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11617A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*587+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.528+4A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*132+4A>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.670+4A>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

11-8148202-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148202
    reference: chr 11
allele count: 4
allele frequency: 3.29733740004946e-5
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15518A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.667+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*587+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.883+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.523+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.670+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11617A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*132+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.528+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.184+4A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.754+4A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.670+4A>G
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-8148212-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148212
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148212
    reference: chr 11
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.748T>G
  hgvsp: ENSP00000431658.1:p.Trp250Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.517T>G
  hgvsp: ENSP00000443871.1:p.Trp173Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*581T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15528T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.178T>G
  hgvsp: ENSP00000379910.2:p.Trp60Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.661T>G
  hgvsp: ENSP00000344904.4:p.Trp221Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.522T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.664T>G
  hgvsp: ENSP00000308820.6:p.Trp222Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11607T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*126T>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.877T>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp222Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS

11-8148214-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148214
    reference: chr 11
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.515A>T
  hgvsp: ENSP00000443871.1:p.Asp172Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11605A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15530A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*579A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.662A>T
  hgvsp: ENSP00000308820.6:p.Asp221Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.659A>T
  hgvsp: ENSP00000344904.4:p.Asp220Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.176A>T
  hgvsp: ENSP00000379910.2:p.Asp59Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.746A>T
  hgvsp: ENSP00000431658.1:p.Asp249Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.520A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.875A>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*124A>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp221Val
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-8148216-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148216
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148216
    reference: chr 11
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.174G>A
  hgvsp: ENST00000396677.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.744G>A
  hgvsp: ENST00000531450.1:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.657G>A
  hgvsp: ENST00000343202.4:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*122G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*577G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.873G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.513G>A
  hgvsp: ENST00000539720.1:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.660G>A
  hgvsp: ENST00000309737.6:c.660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11603G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.518G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15532G>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu220Glu
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

11-8148223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148223
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148223
    reference: chr 11
allele count: 166
allele frequency: 1.367583331960258e-3
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*115A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.737A>G
  hgvsp: ENSP00000431658.1:p.Tyr246Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15539A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.506A>G
  hgvsp: ENSP00000443871.1:p.Tyr169Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11596A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.866A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.511A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*570A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.653A>G
  hgvsp: ENSP00000308820.6:p.Tyr218Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.167A>G
  hgvsp: ENSP00000379910.2:p.Tyr56Cys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.650A>G
  hgvsp: ENSP00000344904.4:p.Tyr217Cys
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 18969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 30715
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr218Cys
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

11-8148228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148228
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148228
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.648C>T
  hgvsp: ENST00000309737.6:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.501C>T
  hgvsp: ENST00000539720.1:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.732C>T
  hgvsp: ENST00000531450.1:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.506C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15544C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.645C>T
  hgvsp: ENST00000343202.4:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*565C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*110C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.861C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.162C>T
  hgvsp: ENST00000396677.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11591C>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala216Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-8148230-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148230
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.643G>T
  hgvsp: ENSP00000344904.4:p.Ala215Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.504G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*108G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.499G>T
  hgvsp: ENSP00000443871.1:p.Ala167Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.730G>T
  hgvsp: ENSP00000431658.1:p.Ala244Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15546G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.646G>T
  hgvsp: ENSP00000308820.6:p.Ala216Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*563G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.859G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.160G>T
  hgvsp: ENSP00000379910.2:p.Ala54Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11589G>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala216Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

11-8148239-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148239
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148239
    reference: chr 11
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11580G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.634G>A
  hgvsp: ENSP00000344904.4:p.Ala212Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.637G>A
  hgvsp: ENSP00000308820.6:p.Ala213Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.495G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.490G>A
  hgvsp: ENSP00000443871.1:p.Ala164Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.721G>A
  hgvsp: ENSP00000431658.1:p.Ala241Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.151G>A
  hgvsp: ENSP00000379910.2:p.Ala51Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.850G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*554G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*99G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15555G>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala213Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

11-8148243-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148243
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148243
    reference: chr 11
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.147A>G
  hgvsp: ENST00000396677.2:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.486A>G
  hgvsp: ENST00000539720.1:c.486A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.630A>G
  hgvsp: ENST00000343202.4:c.630A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15559A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11576A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*550A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.633A>G
  hgvsp: ENST00000309737.6:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.491A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.846A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.717A>G
  hgvsp: ENST00000531450.1:c.717A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*95A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys211Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-8148247-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148247
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148247
    reference: chr 11
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.713A>G
  hgvsp: ENSP00000431658.1:p.Glu238Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11572A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.842A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.482A>G
  hgvsp: ENSP00000443871.1:p.Glu161Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*91A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.629A>G
  hgvsp: ENSP00000308820.6:p.Glu210Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.487A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.626A>G
  hgvsp: ENSP00000344904.4:p.Glu209Gly
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*546A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15563A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.143A>G
  hgvsp: ENSP00000379910.2:p.Glu48Gly
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu210Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

11-8148253-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148253
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148253
    reference: chr 11
allele count: 5
allele frequency: 4.119023297195769e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.620C>T
  hgvsp: ENSP00000344904.4:p.Ser207Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.836C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.137C>T
  hgvsp: ENSP00000379910.2:p.Ser46Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.481C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.707C>T
  hgvsp: ENSP00000431658.1:p.Ser236Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*540C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.476C>T
  hgvsp: ENSP00000443871.1:p.Ser159Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.623C>T
  hgvsp: ENSP00000308820.6:p.Ser208Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15569C>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11566C>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18929
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser208Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-8148256-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148256
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148256
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11563T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.704T>C
  hgvsp: ENSP00000431658.1:p.Phe235Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.833T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.473T>C
  hgvsp: ENSP00000443871.1:p.Phe158Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*537T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.478T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.617T>C
  hgvsp: ENSP00000344904.4:p.Phe206Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*82T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15572T>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.134T>C
  hgvsp: ENSP00000379910.2:p.Phe45Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.620T>C
  hgvsp: ENSP00000308820.6:p.Phe207Ser
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30855
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe207Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

11-8148259-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148259
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148259
    reference: chr 11
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15575G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.701G>C
  hgvsp: ENSP00000431658.1:p.Arg234Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.475G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*79G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.470G>C
  hgvsp: ENSP00000443871.1:p.Arg157Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.131G>C
  hgvsp: ENSP00000379910.2:p.Arg44Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11560G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.614G>C
  hgvsp: ENSP00000344904.4:p.Arg205Thr
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*534G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.830G>C
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.617G>C
  hgvsp: ENSP00000308820.6:p.Arg206Thr
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg206Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-8148259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148259
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148259
    reference: chr 11
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.617G>A
  hgvsp: ENSP00000308820.6:p.Arg206Lys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.131G>A
  hgvsp: ENSP00000379910.2:p.Arg44Lys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15575G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.830G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.614G>A
  hgvsp: ENSP00000344904.4:p.Arg205Lys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.470G>A
  hgvsp: ENSP00000443871.1:p.Arg157Lys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*534G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11560G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.475G>A
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.701G>A
  hgvsp: ENSP00000431658.1:p.Arg234Lys
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*79G>A
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg206Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-8148266-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148266
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148266
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*527A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.607A>G
  hgvsp: ENSP00000344904.4:p.Ile203Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.468A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.694A>G
  hgvsp: ENSP00000431658.1:p.Ile232Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*72A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11553A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.463A>G
  hgvsp: ENSP00000443871.1:p.Ile155Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.124A>G
  hgvsp: ENSP00000379910.2:p.Ile42Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.823A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.610A>G
  hgvsp: ENSP00000308820.6:p.Ile204Val
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15582A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile204Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

11-8148273-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148273
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148273
    reference: chr 11
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.117A>G
  hgvsp: ENST00000396677.2:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.456A>G
  hgvsp: ENST00000539720.1:c.456A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.600A>G
  hgvsp: ENST00000343202.4:c.600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*520A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.687A>G
  hgvsp: ENST00000531450.1:c.687A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15589A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11546A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.816A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*65A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.603A>G
  hgvsp: ENST00000309737.6:c.603A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.461A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly201Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-8148287-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148287
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148287
    reference: chr 11
allele count: 323
allele frequency: 2.660845209654831e-3
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.103G>T
  hgvsp: ENSP00000379910.2:p.Val35Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.802G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.447G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.586G>T
  hgvsp: ENSP00000344904.4:p.Val196Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.673G>T
  hgvsp: ENSP00000431658.1:p.Val225Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.589G>T
  hgvsp: ENSP00000308820.6:p.Val197Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15603G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*506G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*51G>T
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.442G>T
  hgvsp: ENSP00000443871.1:p.Val148Phe
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11532G>T
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 8396
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18870
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30880
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Val197Phe
num of homozygotes: 1
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

11-8148292-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148292
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148292
    reference: chr 11
allele count: 4
allele frequency: 3.295110056675893e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.797C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.98C>G
  hgvsp: ENSP00000379910.2:p.Thr33Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.581C>G
  hgvsp: ENSP00000344904.4:p.Thr194Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.668C>G
  hgvsp: ENSP00000431658.1:p.Thr223Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.442C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11527C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.584C>G
  hgvsp: ENSP00000308820.6:p.Thr195Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*46C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.437C>G
  hgvsp: ENSP00000443871.1:p.Thr146Ser
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*501C>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15608C>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr195Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

11-8148300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8148300
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8148300
    reference: chr 11
allele count: 4
allele frequency: 3.295110056675893e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000308820
  ensembl transcript: ENST00000309737
  gene symbol: RIC3
  hgvsc: ENST00000309737.6:c.576A>G
  hgvsp: ENST00000309737.6:c.576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000431658
  ensembl transcript: ENST00000531450
  gene symbol: RIC3
  hgvsc: ENST00000531450.1:c.660A>G
  hgvsp: ENST00000531450.1:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000395320
  ensembl transcript: ENST00000425599
  gene symbol: RIC3
  hgvsc: ENST00000425599.2:c.427+11519A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000524799
  gene symbol: RIC3
  hgvsc: ENST00000524799.1:n.434A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000333988
  ensembl transcript: ENST00000335425
  gene symbol: RIC3
  hgvsc: ENST00000335425.7:c.125-15616A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166405
  ensembl transcript: ENST00000530060
  gene symbol: RIC3
  hgvsc: ENST00000530060.1:n.789A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000379910
  ensembl transcript: ENST00000396677
  gene symbol: RIC3
  hgvsc: ENST00000396677.2:c.90A>G
  hgvsp: ENST00000396677.2:c.90A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000443871
  ensembl transcript: ENST00000539720
  gene symbol: RIC3
  hgvsc: ENST00000539720.1:c.429A>G
  hgvsp: ENST00000539720.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000344904
  ensembl transcript: ENST00000343202
  gene symbol: RIC3
  hgvsc: ENST00000343202.4:c.573A>G
  hgvsp: ENST00000343202.4:c.573A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000435244
  ensembl transcript: ENST00000528463
  gene symbol: RIC3
  hgvsc: ENST00000528463.1:c.*493A>G
  variant of: http://identifiers.org/hgnc/30338
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000166405
  ensembl protein: ENSP00000434787
  ensembl transcript: ENST00000526962
  gene symbol: RIC3
  hgvsc: ENST00000526962.1:c.*38A>G
  variant of: http://identifiers.org/hgnc/30338
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg192Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP

GenotypeDepth
all individuals: 1525
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

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

GenotypeQuality
all individuals: 3909
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 413
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 359
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13082
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1571
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37144
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.698e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.25e-1

DP
type: SiteQuality
SIO_000300: 1.980673e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.414e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

GenotypeDepth
all individuals: 70
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1567
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13081
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37156
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 525
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.239e-1

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

FS
type: SiteQuality
SIO_000300: 4.544e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 1.980484e6

GenotypeDepth
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3907
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 9.75e1
variant carriers: 4

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

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.980498e6

QD
type: SiteQuality
SIO_000300: 1.31e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
all individuals: 208
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 522
bin: 9.75e1
variant carriers: 2

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

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

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

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

GenotypeQuality
all individuals: 1567
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.980486e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.448e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

FS
type: SiteQuality
SIO_000300: 7.293e0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

GenotypeDepth
all individuals: 5691
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 2.402921953094963e-3
allele num: 10404
num of homozygotes: 0

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

Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.982637e6

QD
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SIO_000300: 1.262e1

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 frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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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: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

African
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East Asian
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South Asian
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Other
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FS
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -3.51e-1

ReadPosRankSum
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SIO_000300: 1.55e0

QD
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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: 1
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allele num: 66734
num of homozygotes: 0

African
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European (Finnish)
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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East Asian
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South Asian
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ClippingRankSum
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SIO_000300: 2.59e-1

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

South Asian
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African
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Other
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European (Finnish)
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.4e-2

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

South Asian
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Other
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East Asian
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Latino
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African
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 22

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

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

East Asian
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allele count: 22
allele frequency: 2.542177027963947e-3
allele num: 8654
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
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SIO_000300: 1.233e1

FS
type: SiteQuality
SIO_000300: 4.235e0

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.057e0

DP
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SIO_000300: 1.979464e6

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
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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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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.118e1

ReadPosRankSum
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SIO_000300: 4.4e-2

FS
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SIO_000300: 2.659e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
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SIO_000300: 1.78e0

BaseQRankSum
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SIO_000300: 7.64e-1

DP
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SIO_000300: 1.975792e6

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

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

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

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

African
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allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.3845e1

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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MQRankSum
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SIO_000300: -1.465e0

ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 1.975692e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.972742e6

FS
type: SiteQuality
SIO_000300: 6.851e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: 2.92e-1

ReadPosRankSum
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SIO_000300: 2.21e0

BaseQRankSum
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SIO_000300: 3.81e0

VQSLOD
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SIO_000300: -4.67e-2

QD
type: SiteQuality
SIO_000300: 1.057e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 3854
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.237164419151305e-4
allele num: 16166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.96278e6

MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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SIO_000300: 6.36e-1

QD
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SIO_000300: 1.342e1

InbreedingCoeff
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SIO_000300: 1.0e-3

BaseQRankSum
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SIO_000300: -4.87e-1

MQ
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GenotypeDepth
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
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
type: Population
allele count: 0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 7.8e-1

BaseQRankSum
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SIO_000300: 2.98e0

InbreedingCoeff
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SIO_000300: 4.8e-3

DP
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SIO_000300: 1.957015e6

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 11

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.202790473899447e-4
allele num: 66512
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

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

Latino
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allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

African
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South Asian
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allele count: 1
allele frequency: 6.246096189881324e-5
allele num: 16010
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MQ
type: SiteQuality
SIO_000300: 5.915e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1537
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.504347564461293e-5
allele num: 66474
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BaseQRankSum
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SIO_000300: -9.22e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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Other
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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DP
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66334
num of homozygotes: 0

African
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

African
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Other
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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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VQSLOD
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DP
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MQRankSum
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QD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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South Asian
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Other
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DP
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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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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Latino
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ClippingRankSum
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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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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African
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ReadPosRankSum
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MQRankSum
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DP
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SIO_000300: 1.874294e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.985e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.315e0

QD
type: SiteQuality
SIO_000300: 1.182e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.81e-1

GenotypeDepth
all individuals: 634
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 406
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
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GenotypeQuality
all individuals: 31454
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3660
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.853008e6

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

VQSLOD
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SIO_000300: -2.491e0

FS
type: SiteQuality
SIO_000300: 2.494e0

MQ
type: SiteQuality
SIO_000300: 5.843e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.202e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.44e-1

GenotypeDepth
all individuals: 18276
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10932
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variant carriers: 0

GenotypeQuality
all individuals: 1100
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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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
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11854
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.077775383952479e-5
allele num: 64982
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 4.423e0

DP
type: SiteQuality
SIO_000300: 1.838916e6

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.189e0

VQSLOD
type: SiteQuality
SIO_000300: -1.966e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 2.39e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

GenotypeDepth
all individuals: 733
bin: 5.25e1
variant carriers: 4

GenotypeDepth
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 6543
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 481
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3328
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3555
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.94743351886209e-4
allele num: 64680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.545117428924598e-4
allele num: 6472
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.098635886673662e-4
allele num: 9530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.95e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.739e0

FS
type: SiteQuality
SIO_000300: 1.854e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 1.818903e6

QD
type: SiteQuality
SIO_000300: 1.326e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

GenotypeQuality
all individuals: 175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4328
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variant carriers: 0

GenotypeQuality
all individuals: 203
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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: 73
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variant carriers: 0

GenotypeQuality
all individuals: 289
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1199
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 5461
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variant carriers: 0

GenotypeQuality
all individuals: 20080
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variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.890469416785207e-5
allele num: 11248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.93e0

VQSLOD
type: SiteQuality
SIO_000300: -9.292e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 1.492968e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

FS
type: SiteQuality
SIO_000300: 3.522e0

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.63e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 241
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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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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62900
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.942334460131238e-5
allele num: 10058
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

BaseQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.186e1

FS
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
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SIO_000300: 8.599999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 69
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.194172438500119e-4
allele num: 8374
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.665718855518038e-4
allele num: 11254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 10058
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VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 2.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
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SIO_000300: 2.99e0

DP
type: SiteQuality
SIO_000300: 1.482764e6

ClippingRankSum
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 202
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 182
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.647744122008049e-5
allele num: 37768
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.319e0

DP
type: SiteQuality
SIO_000300: 1.0431e6

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.288e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.83e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
all individuals: 21525
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
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GenotypeQuality
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GenotypeQuality
all individuals: 460
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GenotypeQuality
all individuals: 830
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GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 1604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.647744122008049e-5
allele num: 37768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.132196162046908e-4
allele num: 4690
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.638e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.83e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.0431e6

VQSLOD
type: SiteQuality
SIO_000300: -2.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.288e0

QD
type: SiteQuality
SIO_000300: 5.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5140
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15989
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3891
bin: 2.25e1
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GenotypeQuality
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1333
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5591
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.333333333333334e-3
allele num: 600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.777822963264199e-5
allele num: 14754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 9.29257e5

GenotypeQuality
all individuals: 3891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5140
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15989
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14630
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1333
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5591
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14754
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.29257e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 7.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 172

GenotypeQuality
all individuals: 1378
bin: 7.75e1
variant carriers: 59

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 39

GenotypeQuality
all individuals: 1676
bin: 5.25e1
variant carriers: 170

GenotypeQuality
all individuals: 1714
bin: 5.75e1
variant carriers: 104

GenotypeQuality
all individuals: 1082
bin: 6.75e1
variant carriers: 104

GenotypeQuality
all individuals: 1784
bin: 1.25e1
variant carriers: 87

GenotypeQuality
all individuals: 1106
bin: 6.25e1
variant carriers: 77

GenotypeQuality
all individuals: 2725
bin: 7.5e0
variant carriers: 89

GenotypeQuality
all individuals: 1387
bin: 2.75e1
variant carriers: 158

GenotypeQuality
all individuals: 22765
bin: 2.5e0
variant carriers: 104

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 101

GenotypeQuality
all individuals: 1289
bin: 4.25e1
variant carriers: 158

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 102

GenotypeQuality
all individuals: 6474
bin: 9.75e1
variant carriers: 215

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 106

GenotypeQuality
all individuals: 1355
bin: 3.25e1
variant carriers: 123

GenotypeQuality
all individuals: 849
bin: 8.25e1
variant carriers: 47

GenotypeQuality
all individuals: 1334
bin: 4.75e1
variant carriers: 185

Latino
type: Population
allele count: 29
allele frequency: 8.252703471826979e-3
allele num: 3514
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 3.313253012048193e-2
allele num: 332
num of homozygotes: 0

East Asian
type: Population
allele count: 29
allele frequency: 1.105182926829268e-2
allele num: 2624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1117
allele frequency: 4.775953480417308e-2
allele num: 23388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 131
allele frequency: 4.378342245989305e-2
allele num: 2992
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 9.269662921348315e-3
allele num: 3560
num of homozygotes: 0

South Asian
type: Population
allele count: 30
allele frequency: 1.1441647597254e-2
allele num: 2622
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

QD
type: SiteQuality
SIO_000300: 8.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 7.62949e5

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
all individuals: 1355
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1289
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1378
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1106
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 849
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1784
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2725
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1387
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1082
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6474
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1714
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1334
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1676
bin: 5.25e1
variant carriers: 6

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.671122994652406e-3
allele num: 2992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 1.368223020352317e-3
allele num: 23388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.810975609756098e-4
allele num: 2624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3514
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.62949e5

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

QD
type: SiteQuality
SIO_000300: 8.34e0

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 776

GenotypeQuality
all individuals: 1784
bin: 1.25e1
variant carriers: 1242

GenotypeQuality
all individuals: 2725
bin: 7.5e0
variant carriers: 1094

GenotypeQuality
all individuals: 1355
bin: 3.25e1
variant carriers: 1113

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 990

GenotypeQuality
all individuals: 22765
bin: 2.5e0
variant carriers: 1047

GenotypeQuality
all individuals: 1387
bin: 2.75e1
variant carriers: 1131

GenotypeQuality
all individuals: 6474
bin: 9.75e1
variant carriers: 6151

GenotypeQuality
all individuals: 1289
bin: 4.25e1
variant carriers: 1090

GenotypeQuality
all individuals: 1714
bin: 5.75e1
variant carriers: 1581

GenotypeQuality
all individuals: 1082
bin: 6.75e1
variant carriers: 953

GenotypeQuality
all individuals: 1378
bin: 7.75e1
variant carriers: 1271

GenotypeQuality
all individuals: 1334
bin: 4.75e1
variant carriers: 1125

GenotypeQuality
all individuals: 1106
bin: 6.25e1
variant carriers: 997

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 1034

GenotypeQuality
all individuals: 1676
bin: 5.25e1
variant carriers: 1483

GenotypeQuality
all individuals: 849
bin: 8.25e1
variant carriers: 757

GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 1044

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 655

African
type: Population
allele count: 1581
allele frequency: 4.441011235955056e-1
allele num: 3560
num of homozygotes: 65

European (Non-Finnish)
type: Population
allele count: 10304
allele frequency: 4.405678125534462e-1
allele num: 23388
num of homozygotes: 253

Latino
type: Population
allele count: 1709
allele frequency: 4.863403528742174e-1
allele num: 3514
num of homozygotes: 43

European (Finnish)
type: Population
allele count: 1378
allele frequency: 4.605614973262032e-1
allele num: 2992
num of homozygotes: 54

East Asian
type: Population
allele count: 1280
allele frequency: 4.878048780487805e-1
allele num: 2624
num of homozygotes: 33

South Asian
type: Population
allele count: 1281
allele frequency: 4.88558352402746e-1
allele num: 2622
num of homozygotes: 29

Other
type: Population
allele count: 154
allele frequency: 4.63855421686747e-1
allele num: 332
num of homozygotes: 8

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

DP
type: SiteQuality
SIO_000300: 7.62949e5

GenotypeQuality
all individuals: 22765
bin: 2.5e0
variant carriers: 69

GenotypeQuality
all individuals: 1106
bin: 6.25e1
variant carriers: 50

GenotypeQuality
all individuals: 849
bin: 8.25e1
variant carriers: 48

GenotypeQuality
all individuals: 2725
bin: 7.5e0
variant carriers: 70

GenotypeQuality
all individuals: 1355
bin: 3.25e1
variant carriers: 65

GenotypeQuality
all individuals: 1676
bin: 5.25e1
variant carriers: 58

GenotypeQuality
all individuals: 1334
bin: 4.75e1
variant carriers: 68

GenotypeQuality
all individuals: 1405
bin: 1.75e1
variant carriers: 78

GenotypeQuality
all individuals: 1289
bin: 4.25e1
variant carriers: 82

GenotypeQuality
all individuals: 1784
bin: 1.25e1
variant carriers: 79

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 38

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 88

GenotypeQuality
all individuals: 6474
bin: 9.75e1
variant carriers: 147

GenotypeQuality
all individuals: 1082
bin: 6.75e1
variant carriers: 35

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 58

GenotypeQuality
all individuals: 1286
bin: 3.75e1
variant carriers: 63

GenotypeQuality
all individuals: 1387
bin: 2.75e1
variant carriers: 56

GenotypeQuality
all individuals: 1378
bin: 7.75e1
variant carriers: 47

GenotypeQuality
all individuals: 836
bin: 9.25e1
variant carriers: 23

South Asian
type: Population
allele count: 72
allele frequency: 2.745995423340961e-2
allele num: 2622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 18
allele frequency: 6.016042780748663e-3
allele num: 2992
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 1.204819277108434e-2
allele num: 332
num of homozygotes: 0

Latino
type: Population
allele count: 98
allele frequency: 2.788844621513944e-2
allele num: 3514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 446
allele frequency: 1.906960834616043e-2
allele num: 23388
num of homozygotes: 0

African
type: Population
allele count: 87
allele frequency: 2.443820224719101e-2
allele num: 3560
num of homozygotes: 0

East Asian
type: Population
allele count: 60
allele frequency: 2.286585365853658e-2
allele num: 2624
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.34e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 7.62949e5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2624
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 7.627765064836003e-4
allele num: 2622
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.808988764044944e-4
allele num: 3560
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

DP
type: SiteQuality
SIO_000300: 7.62949e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

Latino
type: Population
allele count: 4
allele frequency: 1.138303927148549e-3
allele num: 3514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 9.406533264922182e-4
allele num: 23388
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.1441647597254e-3
allele num: 2622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.62949e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 8.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 374
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6713
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2628
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1371
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4540
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4346
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.809103408350821e-5
allele num: 55276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.047e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

MQRankSum
type: SiteQuality
SIO_000300: -1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -1.753e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.903e0

DP
type: SiteQuality
SIO_000300: 1.066867e6

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

GenotypeQuality
all individuals: 3318
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 362
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 1513
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 7086
bin: 3.25e1
variant carriers: 12

GenotypeQuality
all individuals: 1161
bin: 7.25e1
variant carriers: 18

GenotypeQuality
all individuals: 3008
bin: 4.25e1
variant carriers: 24

GenotypeQuality
all individuals: 7680
bin: 2.25e1
variant carriers: 12

GenotypeQuality
all individuals: 783
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2529
bin: 1.75e1
variant carriers: 18

GenotypeQuality
all individuals: 5575
bin: 6.25e1
variant carriers: 11

GenotypeQuality
all individuals: 452
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variant carriers: 13

GenotypeQuality
all individuals: 362
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 6657
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 4346
bin: 4.75e1
variant carriers: 15

GenotypeQuality
all individuals: 2915
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 2738
bin: 9.75e1
variant carriers: 685

GenotypeQuality
all individuals: 4423
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1390
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 871
bin: 8.25e1
variant carriers: 20

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.624021076184633e-4
allele num: 55418
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 6.983240223463687e-3
allele num: 716
num of homozygotes: 0

African
type: Population
allele count: 796
allele frequency: 9.846610588817417e-2
allele num: 8084
num of homozygotes: 43

Latino
type: Population
allele count: 44
allele frequency: 4.223459397197159e-3
allele num: 10418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.778e0

QD
type: SiteQuality
SIO_000300: 2.009e1

VQSLOD
type: SiteQuality
SIO_000300: -7.746e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.77e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.062579e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

GenotypeQuality
all individuals: 339
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 520
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
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GenotypeQuality
all individuals: 6903
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.644e0

MQRankSum
type: SiteQuality
SIO_000300: 9.87e-1

QD
type: SiteQuality
SIO_000300: 9.640000000000001e0

DP
type: SiteQuality
SIO_000300: 1.632002e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

FS
type: SiteQuality
SIO_000300: 2.418e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 6845
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 338
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 319
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 241
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 44350
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 458
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 9.75e1
variant carriers: 1488

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 1

South Asian
type: Population
allele count: 90
allele frequency: 5.53982518773852e-3
allele num: 16246
num of homozygotes: 1

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

Other
type: Population
allele count: 5
allele frequency: 5.543237250554324e-3
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 645
allele frequency: 6.229476530809349e-2
allele num: 10354
num of homozygotes: 25

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

Latino
type: Population
allele count: 723
allele frequency: 6.256490134994808e-2
allele num: 11556
num of homozygotes: 21

European (Non-Finnish)
type: Population
allele count: 85
allele frequency: 1.277657527657528e-3
allele num: 66528
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

DP
type: SiteQuality
SIO_000300: 1.656467e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.24e0

QD
type: SiteQuality
SIO_000300: 1.543e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.97e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 258
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variant carriers: 0

GenotypeQuality
all individuals: 46761
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 268
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 1489
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variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
all individuals: 1386
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
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GenotypeQuality
all individuals: 1474
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 6995
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.460207612456747e-4
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.182e0

DP
type: SiteQuality
SIO_000300: 1.634459e6

VQSLOD
type: SiteQuality
SIO_000300: -1.194e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

FS
type: SiteQuality
SIO_000300: 6.44e-1

QD
type: SiteQuality
SIO_000300: 7.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeDepth
all individuals: 62
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
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variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 48005
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variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 237
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.647715e6

QD
type: SiteQuality
SIO_000300: 1.524e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.725e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeDepth
all individuals: 34
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 0
bin: 1.75e1
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GenotypeQuality
all individuals: 237
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GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1466
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 7073
bin: 6.75e1
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GenotypeQuality
all individuals: 610
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GenotypeQuality
all individuals: 55
bin: 2.25e1
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GenotypeQuality
all individuals: 48069
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

FS
type: SiteQuality
SIO_000300: 1.184e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

QD
type: SiteQuality
SIO_000300: 1.395e1

VQSLOD
type: SiteQuality
SIO_000300: 8.84e-1

DP
type: SiteQuality
SIO_000300: 1.648527e6

GenotypeDepth
all individuals: 62
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 1482
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GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 7073
bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.499775011249437e-5
allele num: 66670
num of homozygotes: 0

QD
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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SIO_000300: 8.84e-1

InbreedingCoeff
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SIO_000300: 1.34e-2

MQ
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FS
type: SiteQuality
SIO_000300: 1.184e0

MQRankSum
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SIO_000300: -3.39e-1

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
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allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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

DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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SIO_000300: 2.881e0

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

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

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

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

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

European (Non-Finnish)
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allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

MQRankSum
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DP
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QD
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VQSLOD
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -7.68e-1

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

Latino
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allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 1

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

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

Other
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allele 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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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QD
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MQ
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SIO_000300: 5.931e1

DP
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InbreedingCoeff
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SIO_000300: 7.64e-2

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele count: 8
allele frequency: 6.91323885240235e-4
allele num: 11572
num of homozygotes: 0

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

African
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allele count: 157
allele frequency: 1.509034986543637e-2
allele num: 10404
num of homozygotes: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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

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

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

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

Latino
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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East Asian
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DP
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

South Asian
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Other
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European (Finnish)
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.647313e6

QD
type: SiteQuality
SIO_000300: 1.287e1

BaseQRankSum
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SIO_000300: -1.706e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.13e-1

FS
type: SiteQuality
SIO_000300: 1.446e0

MQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

DP
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SIO_000300: 1.647355e6

FS
type: SiteQuality
SIO_000300: 4.936e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.495e1

ReadPosRankSum
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SIO_000300: 8.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.6474e6

BaseQRankSum
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SIO_000300: -1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.47e-1

FS
type: SiteQuality
SIO_000300: 6.67e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
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GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.32152117545376e-4
allele num: 11570
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.456e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

FS
type: SiteQuality
SIO_000300: 9.53e-1

MQRankSum
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SIO_000300: 7.85e-1

ReadPosRankSum
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SIO_000300: 1.03e0

QD
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SIO_000300: 1.096e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 1.647467e6

GenotypeQuality
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bin: 5.25e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

African
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allele count: 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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.647408e6

ClippingRankSum
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SIO_000300: 1.03e-1

MQRankSum
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SIO_000300: -9.9e-2

VQSLOD
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SIO_000300: 3.01e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 7.018e0

ReadPosRankSum
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SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

Latino
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allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

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

South Asian
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MQRankSum
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SIO_000300: -4.85e-1

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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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10406
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East Asian
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allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.293e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.647425e6

QD
type: SiteQuality
SIO_000300: 1.617e1

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1450
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1490
bin: 9.75e1
variant carriers: 322

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

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

GenotypeQuality
all individuals: 7028
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48397
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.32152117545376e-4
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 149
allele frequency: 2.252797097066828e-2
allele num: 6614
num of homozygotes: 1

Other
type: Population
allele count: 4
allele frequency: 4.415011037527594e-3
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 161
allele frequency: 2.412635617095247e-3
allele num: 66732
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.777e0

QD
type: SiteQuality
SIO_000300: 1.326e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.659245e6

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48681
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1335
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 1450
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

FS
type: SiteQuality
SIO_000300: 5.745e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.44e1

DP
type: SiteQuality
SIO_000300: 1.642813e6

GenotypeQuality
all individuals: 1171
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 48693
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 562
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7055
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 199
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.108e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

DP
type: SiteQuality
SIO_000300: 1.642874e6