6-36168411-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168411
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168411
    reference: chr 6
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.312C>T
  hgvsp: ENST00000532330.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.312C>T
  hgvsp: ENST00000543502.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.312C>T
  hgvsp: ENST00000534694.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.312C>T
  hgvsp: ENST00000534400.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.312C>T
  hgvsp: ENST00000357641.6:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.312C>T
  hgvsp: ENST00000339717.7:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.229C>T
  hgvsp: ENST00000441123.1:c.229C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.312C>T
  hgvsp: ENST00000449261.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.312C>T
  hgvsp: ENST00000454960.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.312C>T
  hgvsp: ENST00000443324.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser104Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

6-36168413-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168413
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168413
    reference: chr 6
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.314A>G
  hgvsp: ENSP00000413655.1:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.314A>G
  hgvsp: ENSP00000387368.2:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.314A>G
  hgvsp: ENSP00000436504.1:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.314A>G
  hgvsp: ENSP00000434501.1:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.314A>G
  hgvsp: ENSP00000437087.1:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.314A>G
  hgvsp: ENSP00000445352.1:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.231A>G
  hgvsp: ENSP00000411558.1:p.Lys78Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.314A>G
  hgvsp: ENSP00000350267.6:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.314A>G
  hgvsp: ENSP00000345419.7:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.314A>G
  hgvsp: ENSP00000416842.2:p.Lys105Arg
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys105Arg
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-36168415-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168415
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168415
    reference: chr 6
allele count: 44
allele frequency: 3.634261171223259e-4
allele num: 121070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.316C>T
  hgvsp: ENSP00000416842.2:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.316C>T
  hgvsp: ENSP00000434501.1:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.316C>T
  hgvsp: ENSP00000445352.1:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.316C>T
  hgvsp: ENSP00000437087.1:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.316C>T
  hgvsp: ENSP00000436504.1:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.316C>T
  hgvsp: ENSP00000345419.7:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.316C>T
  hgvsp: ENSP00000387368.2:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.233C>T
  hgvsp: ENSP00000411558.1:p.His79Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.316C>T
  hgvsp: ENSP00000350267.6:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.316C>T
  hgvsp: ENSP00000413655.1:p.His106Tyr
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 38073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.His106Tyr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD

6-36168423-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168423
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168423
    reference: chr 6
allele count: 2
allele frequency: 1.652073352056831e-5
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.324T>G
  hgvsp: ENST00000534694.1:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.324T>G
  hgvsp: ENST00000532330.1:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.241T>G
  hgvsp: ENST00000441123.1:c.241T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.324T>G
  hgvsp: ENST00000357641.6:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.324T>G
  hgvsp: ENST00000543502.1:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.324T>G
  hgvsp: ENST00000449261.2:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.324T>G
  hgvsp: ENST00000534400.1:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.324T>G
  hgvsp: ENST00000443324.2:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.324T>G
  hgvsp: ENST00000339717.7:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.324T>G
  hgvsp: ENST00000454960.1:c.324T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser108Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

6-36168436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168436
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168436
    reference: chr 6
allele count: 3
allele frequency: 2.4786014078456e-5
allele num: 121036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.337C>T
  hgvsp: ENSP00000436504.1:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.337C>T
  hgvsp: ENSP00000350267.6:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.337C>T
  hgvsp: ENSP00000387368.2:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.337C>T
  hgvsp: ENSP00000445352.1:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.254C>T
  hgvsp: ENSP00000411558.1:p.His86Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.337C>T
  hgvsp: ENSP00000416842.2:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.337C>T
  hgvsp: ENSP00000437087.1:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.337C>T
  hgvsp: ENSP00000413655.1:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.337C>T
  hgvsp: ENSP00000434501.1:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.337C>T
  hgvsp: ENSP00000345419.7:p.His113Tyr
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His113Tyr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

6-36168451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168451
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168451
    reference: chr 6
allele count: 1
allele frequency: 8.260776182530111e-6
allele num: 121054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.352A>G
  hgvsp: ENSP00000436504.1:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.352A>G
  hgvsp: ENSP00000445352.1:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.352A>G
  hgvsp: ENSP00000434501.1:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.352A>G
  hgvsp: ENSP00000350267.6:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.352A>G
  hgvsp: ENSP00000345419.7:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.352A>G
  hgvsp: ENSP00000413655.1:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.269A>G
  hgvsp: ENSP00000411558.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.352A>G
  hgvsp: ENSP00000416842.2:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.352A>G
  hgvsp: ENSP00000437087.1:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.352A>G
  hgvsp: ENSP00000387368.2:p.Ser118Gly
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser118Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-36168458-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168458
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168458
    reference: chr 6
allele count: 3
allele frequency: 2.478110028085247e-5
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.359G>A
  hgvsp: ENSP00000445352.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.359G>A
  hgvsp: ENSP00000416842.2:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.359G>A
  hgvsp: ENSP00000413655.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.359G>A
  hgvsp: ENSP00000350267.6:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.359G>A
  hgvsp: ENSP00000436504.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.359G>A
  hgvsp: ENSP00000434501.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.359G>A
  hgvsp: ENSP00000387368.2:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.359G>A
  hgvsp: ENSP00000345419.7:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.359G>A
  hgvsp: ENSP00000437087.1:p.Arg120His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.276G>A
  hgvsp: ENSP00000411558.1:p.Arg93His
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg120His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

6-36168458-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168458
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168458
    reference: chr 6
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.359G>T
  hgvsp: ENSP00000434501.1:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.359G>T
  hgvsp: ENSP00000437087.1:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.359G>T
  hgvsp: ENSP00000413655.1:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.359G>T
  hgvsp: ENSP00000350267.6:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.359G>T
  hgvsp: ENSP00000345419.7:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.359G>T
  hgvsp: ENSP00000445352.1:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.359G>T
  hgvsp: ENSP00000416842.2:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.276G>T
  hgvsp: ENSP00000411558.1:p.Arg93Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.359G>T
  hgvsp: ENSP00000436504.1:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.359G>T
  hgvsp: ENSP00000387368.2:p.Arg120Leu
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15247
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg120Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

6-36168480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168480
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168480
    reference: chr 6
allele count: 2
allele frequency: 1.651391297167864e-5
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.381G>A
  hgvsp: ENST00000543502.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.381G>A
  hgvsp: ENST00000443324.2:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.381G>A
  hgvsp: ENST00000534694.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.381G>A
  hgvsp: ENST00000532330.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.381G>A
  hgvsp: ENST00000357641.6:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.381G>A
  hgvsp: ENST00000339717.7:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.381G>A
  hgvsp: ENST00000449261.2:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000413655
  ensembl transcript: ENST00000454960
  gene symbol: BRPF3
  hgvsc: ENST00000454960.1:c.381G>A
  hgvsp: ENST00000454960.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.298G>A
  hgvsp: ENST00000441123.1:c.298G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.381G>A
  hgvsp: ENST00000534400.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln127Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

6-36168492-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168492
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168492
    reference: chr 6
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.393C>G
  hgvsp: ENST00000543502.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.393C>G
  hgvsp: ENST00000534400.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.393C>G
  hgvsp: ENST00000534694.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.393C>G
  hgvsp: ENST00000357641.6:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.310C>G
  hgvsp: ENST00000441123.1:c.310C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.393C>G
  hgvsp: ENST00000532330.1:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.393C>G
  hgvsp: ENST00000449261.2:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.393C>G
  hgvsp: ENST00000339717.7:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.393C>G
  hgvsp: ENST00000443324.2:c.393C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro131Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-36168494-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168494
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168494
    reference: chr 6
allele count: 3
allele frequency: 2.475942095967516e-5
allele num: 121166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.312C>T
  hgvsp: ENSP00000411558.1:p.Pro105Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.395C>T
  hgvsp: ENSP00000445352.1:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.395C>T
  hgvsp: ENSP00000437087.1:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.395C>T
  hgvsp: ENSP00000436504.1:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.395C>T
  hgvsp: ENSP00000416842.2:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.395C>T
  hgvsp: ENSP00000350267.6:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.395C>T
  hgvsp: ENSP00000345419.7:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.395C>T
  hgvsp: ENSP00000387368.2:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.395C>T
  hgvsp: ENSP00000434501.1:p.Pro132Leu
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro132Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-36168495-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168495
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168495
    reference: chr 6
allele count: 4
allele frequency: 3.301528607745386e-5
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.396G>A
  hgvsp: ENST00000443324.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.396G>A
  hgvsp: ENST00000357641.6:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.396G>A
  hgvsp: ENST00000339717.7:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.396G>A
  hgvsp: ENST00000543502.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.396G>A
  hgvsp: ENST00000534694.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.396G>A
  hgvsp: ENST00000534400.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.396G>A
  hgvsp: ENST00000532330.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.396G>A
  hgvsp: ENST00000449261.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.313G>A
  hgvsp: ENST00000441123.1:c.313G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro132Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

6-36168513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168513
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168513
    reference: chr 6
allele count: 144
allele frequency: 1.18790318589035e-3
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.414C>T
  hgvsp: ENST00000443324.2:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.414C>T
  hgvsp: ENST00000532330.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.414C>T
  hgvsp: ENST00000543502.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.414C>T
  hgvsp: ENST00000534400.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.331C>T
  hgvsp: ENST00000441123.1:c.331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.414C>T
  hgvsp: ENST00000534694.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.414C>T
  hgvsp: ENST00000357641.6:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.414C>T
  hgvsp: ENST00000449261.2:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.414C>T
  hgvsp: ENST00000339717.7:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 15336
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 38130
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 9.75e1
  variant carriers: 144
genotype quality: GenotypeQuality
  all individuals: 43723
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr138Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

6-36168515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168515
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168515
    reference: chr 6
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.416G>A
  hgvsp: ENSP00000437087.1:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.416G>A
  hgvsp: ENSP00000445352.1:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.416G>A
  hgvsp: ENSP00000350267.6:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.416G>A
  hgvsp: ENSP00000416842.2:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.333G>A
  hgvsp: ENSP00000411558.1:p.Arg112His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.416G>A
  hgvsp: ENSP00000434501.1:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.416G>A
  hgvsp: ENSP00000387368.2:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.416G>A
  hgvsp: ENSP00000345419.7:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.416G>A
  hgvsp: ENSP00000436504.1:p.Arg139His
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg139His
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-36168519-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168519
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168519
    reference: chr 6
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.420C>T
  hgvsp: ENST00000357641.6:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.420C>T
  hgvsp: ENST00000534400.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.420C>T
  hgvsp: ENST00000449261.2:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.420C>T
  hgvsp: ENST00000532330.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.420C>T
  hgvsp: ENST00000339717.7:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.420C>T
  hgvsp: ENST00000534694.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.337C>T
  hgvsp: ENST00000441123.1:c.337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.420C>T
  hgvsp: ENST00000543502.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.420C>T
  hgvsp: ENST00000443324.2:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr140Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

6-36168525-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168525
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168525
    reference: chr 6
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.426G>A
  hgvsp: ENST00000543502.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.426G>A
  hgvsp: ENST00000443324.2:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.426G>A
  hgvsp: ENST00000357641.6:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.343G>A
  hgvsp: ENST00000441123.1:c.343G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.426G>A
  hgvsp: ENST00000534400.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.426G>A
  hgvsp: ENST00000449261.2:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.426G>A
  hgvsp: ENST00000532330.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.426G>A
  hgvsp: ENST00000534694.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.426G>A
  hgvsp: ENST00000339717.7:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu142Glu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-36168553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168553
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168553
    reference: chr 6
allele count: 11
allele frequency: 9.067528356634133e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.454G>A
  hgvsp: ENSP00000350267.6:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.454G>A
  hgvsp: ENSP00000387368.2:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.454G>A
  hgvsp: ENSP00000434501.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.454G>A
  hgvsp: ENSP00000445352.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.454G>A
  hgvsp: ENSP00000416842.2:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.454G>A
  hgvsp: ENSP00000436504.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.454G>A
  hgvsp: ENSP00000437087.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.454G>A
  hgvsp: ENSP00000345419.7:p.Val152Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.371G>A
  hgvsp: ENSP00000411558.1:p.Val125Ile
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val152Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-36168561-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168561
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168561
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.462T>C
  hgvsp: ENST00000443324.2:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.462T>C
  hgvsp: ENST00000449261.2:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.462T>C
  hgvsp: ENST00000339717.7:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.379T>C
  hgvsp: ENST00000441123.1:c.379T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.462T>C
  hgvsp: ENST00000357641.6:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.462T>C
  hgvsp: ENST00000543502.1:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.462T>C
  hgvsp: ENST00000532330.1:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.462T>C
  hgvsp: ENST00000534694.1:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.462T>C
  hgvsp: ENST00000534400.1:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15504
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr154Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

6-36168576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168576
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168576
    reference: chr 6
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.477G>A
  hgvsp: ENST00000532330.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.477G>A
  hgvsp: ENST00000543502.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.394G>A
  hgvsp: ENST00000441123.1:c.394G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.477G>A
  hgvsp: ENST00000339717.7:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.477G>A
  hgvsp: ENST00000357641.6:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.477G>A
  hgvsp: ENST00000534400.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.477G>A
  hgvsp: ENST00000449261.2:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.477G>A
  hgvsp: ENST00000534694.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.477G>A
  hgvsp: ENST00000443324.2:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43924
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu159Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

6-36168591-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168591
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168591
    reference: chr 6
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.492G>A
  hgvsp: ENST00000534694.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.409G>A
  hgvsp: ENST00000441123.1:c.409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.492G>A
  hgvsp: ENST00000443324.2:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.492G>A
  hgvsp: ENST00000534400.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.492G>A
  hgvsp: ENST00000339717.7:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.492G>A
  hgvsp: ENST00000357641.6:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.492G>A
  hgvsp: ENST00000449261.2:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.492G>A
  hgvsp: ENST00000532330.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.492G>A
  hgvsp: ENST00000543502.1:c.492G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu164Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-36168595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168595
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168595
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.496A>G
  hgvsp: ENSP00000436504.1:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.496A>G
  hgvsp: ENSP00000434501.1:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.496A>G
  hgvsp: ENSP00000387368.2:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.496A>G
  hgvsp: ENSP00000445352.1:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.496A>G
  hgvsp: ENSP00000416842.2:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.413A>G
  hgvsp: ENSP00000411558.1:p.Met139Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.496A>G
  hgvsp: ENSP00000437087.1:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.496A>G
  hgvsp: ENSP00000345419.7:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.496A>G
  hgvsp: ENSP00000350267.6:p.Met166Val
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43889
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met166Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

6-36168597-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168597
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168597
    reference: chr 6
allele count: 10
allele frequency: 8.238861059847087e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.498G>A
  hgvsp: ENSP00000350267.6:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.498G>A
  hgvsp: ENSP00000416842.2:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.498G>A
  hgvsp: ENSP00000434501.1:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.498G>A
  hgvsp: ENSP00000437087.1:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.498G>A
  hgvsp: ENSP00000345419.7:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.415G>A
  hgvsp: ENSP00000411558.1:p.Met139Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.498G>A
  hgvsp: ENSP00000387368.2:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.498G>A
  hgvsp: ENSP00000445352.1:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.498G>A
  hgvsp: ENSP00000436504.1:p.Met166Ile
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 9.75e1
  variant carriers: 10
hgvs: p.Met166Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

6-36168603-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168603
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168603
    reference: chr 6
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.504T>C
  hgvsp: ENST00000532330.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.504T>C
  hgvsp: ENST00000443324.2:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.504T>C
  hgvsp: ENST00000543502.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.504T>C
  hgvsp: ENST00000534694.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.504T>C
  hgvsp: ENST00000357641.6:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.504T>C
  hgvsp: ENST00000339717.7:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.504T>C
  hgvsp: ENST00000534400.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.421T>C
  hgvsp: ENST00000441123.1:c.421T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.504T>C
  hgvsp: ENST00000449261.2:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15710
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn168Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-36168605-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168605
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168605
    reference: chr 6
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.506A>G
  hgvsp: ENSP00000416842.2:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.506A>G
  hgvsp: ENSP00000437087.1:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.506A>G
  hgvsp: ENSP00000434501.1:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.506A>G
  hgvsp: ENSP00000387368.2:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.506A>G
  hgvsp: ENSP00000350267.6:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.506A>G
  hgvsp: ENSP00000436504.1:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.506A>G
  hgvsp: ENSP00000445352.1:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.506A>G
  hgvsp: ENSP00000345419.7:p.Glu169Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.423A>G
  hgvsp: ENSP00000411558.1:p.Glu142Gly
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu169Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/6-36168608-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168608
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168608
    reference: chr 6
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.509A>C
  hgvsp: ENSP00000350267.6:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.509A>C
  hgvsp: ENSP00000437087.1:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.509A>C
  hgvsp: ENSP00000436504.1:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.509A>C
  hgvsp: ENSP00000434501.1:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.509A>C
  hgvsp: ENSP00000345419.7:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.509A>C
  hgvsp: ENSP00000416842.2:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.509A>C
  hgvsp: ENSP00000445352.1:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.509A>C
  hgvsp: ENSP00000387368.2:p.Lys170Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.426A>C
  hgvsp: ENSP00000411558.1:p.Lys143Thr
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys170Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

6-36168610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168610
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168610
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.511C>T
  hgvsp: ENSP00000387368.2:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.511C>T
  hgvsp: ENSP00000434501.1:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.511C>T
  hgvsp: ENSP00000436504.1:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.511C>T
  hgvsp: ENSP00000345419.7:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.511C>T
  hgvsp: ENSP00000416842.2:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.511C>T
  hgvsp: ENSP00000437087.1:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.511C>T
  hgvsp: ENSP00000350267.6:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.428C>T
  hgvsp: ENSP00000411558.1:p.Arg144Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.511C>T
  hgvsp: ENSP00000445352.1:p.Arg171Trp
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg171Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

6-36168614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168614
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168614
    reference: chr 6
allele count: 16
allele frequency: 1.318022307527555e-4
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.515G>A
  hgvsp: ENSP00000416842.2:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.515G>A
  hgvsp: ENSP00000445352.1:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.515G>A
  hgvsp: ENSP00000350267.6:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.515G>A
  hgvsp: ENSP00000345419.7:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.515G>A
  hgvsp: ENSP00000387368.2:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.515G>A
  hgvsp: ENSP00000437087.1:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.515G>A
  hgvsp: ENSP00000436504.1:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.515G>A
  hgvsp: ENSP00000434501.1:p.Arg172Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.432G>A
  hgvsp: ENSP00000411558.1:p.Arg145Gln
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg172Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/6-36168620-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168620
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168620
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.521A>C
  hgvsp: ENSP00000434501.1:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.521A>C
  hgvsp: ENSP00000436504.1:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.521A>C
  hgvsp: ENSP00000350267.6:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.521A>C
  hgvsp: ENSP00000345419.7:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.521A>C
  hgvsp: ENSP00000445352.1:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.521A>C
  hgvsp: ENSP00000387368.2:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.521A>C
  hgvsp: ENSP00000437087.1:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.438A>C
  hgvsp: ENSP00000411558.1:p.Asp147Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.521A>C
  hgvsp: ENSP00000416842.2:p.Asp174Ala
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp174Ala
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

6-36168628-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168628
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168628
    reference: chr 6
allele count: 7668
allele frequency: 6.317350469599604e-2
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.446A>G
  hgvsp: ENSP00000411558.1:p.Ser150Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.529A>G
  hgvsp: ENSP00000345419.7:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.529A>G
  hgvsp: ENSP00000350267.6:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.529A>G
  hgvsp: ENSP00000437087.1:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.529A>G
  hgvsp: ENSP00000387368.2:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.529A>G
  hgvsp: ENSP00000434501.1:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.529A>G
  hgvsp: ENSP00000445352.1:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.529A>G
  hgvsp: ENSP00000436504.1:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.529A>G
  hgvsp: ENSP00000416842.2:p.Ser177Gly
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 9.75e1
  variant carriers: 1312
genotype depth: GenotypeDepth
  all individuals: 33394
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 6.25e1
  variant carriers: 674
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.25e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 677
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.75e1
  variant carriers: 447
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.75e1
  variant carriers: 593
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.75e1
  variant carriers: 721
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14293
  bin: 2.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 3.25e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 6.75e1
  variant carriers: 591
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 526
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.75e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.25e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 250
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser177Gly
num of homozygotes: 342
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-36168642-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168642
    reference: chr 6
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.543A>G
  hgvsp: ENST00000543502.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.460A>G
  hgvsp: ENST00000441123.1:c.460A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.543A>G
  hgvsp: ENST00000339717.7:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.543A>G
  hgvsp: ENST00000534694.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.543A>G
  hgvsp: ENST00000534400.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.543A>G
  hgvsp: ENST00000449261.2:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.543A>G
  hgvsp: ENST00000532330.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.543A>G
  hgvsp: ENST00000357641.6:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.543A>G
  hgvsp: ENST00000443324.2:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala181Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

6-36168651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168651
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168651
    reference: chr 6
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.552T>C
  hgvsp: ENST00000532330.1:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.552T>C
  hgvsp: ENST00000534400.1:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.552T>C
  hgvsp: ENST00000357641.6:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.469T>C
  hgvsp: ENST00000441123.1:c.469T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.552T>C
  hgvsp: ENST00000534694.1:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.552T>C
  hgvsp: ENST00000443324.2:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.552T>C
  hgvsp: ENST00000543502.1:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.552T>C
  hgvsp: ENST00000449261.2:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.552T>C
  hgvsp: ENST00000339717.7:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34221
  bin: 2.25e1
  variant carriers: 0
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: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43482
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe184Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD

6-36168661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168661
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168661
    reference: chr 6
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.562G>A
  hgvsp: ENSP00000416842.2:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.562G>A
  hgvsp: ENSP00000437087.1:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.479G>A
  hgvsp: ENSP00000411558.1:p.Val161Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.562G>A
  hgvsp: ENSP00000387368.2:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.562G>A
  hgvsp: ENSP00000350267.6:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.562G>A
  hgvsp: ENSP00000434501.1:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.562G>A
  hgvsp: ENSP00000445352.1:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.562G>A
  hgvsp: ENSP00000436504.1:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.562G>A
  hgvsp: ENSP00000345419.7:p.Val188Ile
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val188Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

6-36168668-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168668
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168668
    reference: chr 6
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.569G>A
  hgvsp: ENSP00000387368.2:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.569G>A
  hgvsp: ENSP00000437087.1:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.569G>A
  hgvsp: ENSP00000434501.1:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.569G>A
  hgvsp: ENSP00000436504.1:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.569G>A
  hgvsp: ENSP00000350267.6:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.486G>A
  hgvsp: ENSP00000411558.1:p.Arg163Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.569G>A
  hgvsp: ENSP00000445352.1:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.569G>A
  hgvsp: ENSP00000416842.2:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.569G>A
  hgvsp: ENSP00000345419.7:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg190Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-36168681-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168681
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168681
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.582G>A
  hgvsp: ENST00000449261.2:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.582G>A
  hgvsp: ENST00000532330.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.582G>A
  hgvsp: ENST00000339717.7:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.582G>A
  hgvsp: ENST00000543502.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.582G>A
  hgvsp: ENST00000534400.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.582G>A
  hgvsp: ENST00000357641.6:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.582G>A
  hgvsp: ENST00000534694.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.582G>A
  hgvsp: ENST00000443324.2:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.499G>A
  hgvsp: ENST00000441123.1:c.499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43453
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu194Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-36168697-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168697
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168697
    reference: chr 6
allele count: 4
allele frequency: 3.294784356363876e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.598C>T
  hgvsp: ENSP00000436504.1:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.598C>T
  hgvsp: ENSP00000416842.2:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.515C>T
  hgvsp: ENSP00000411558.1:p.Arg173Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.598C>T
  hgvsp: ENSP00000434501.1:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.598C>T
  hgvsp: ENSP00000437087.1:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.598C>T
  hgvsp: ENSP00000445352.1:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.598C>T
  hgvsp: ENSP00000350267.6:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.598C>T
  hgvsp: ENSP00000345419.7:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.598C>T
  hgvsp: ENSP00000387368.2:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg200Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

6-36168698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168698
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168698
    reference: chr 6
allele count: 11
allele frequency: 9.060507717905211e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.599G>A
  hgvsp: ENSP00000350267.6:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.599G>A
  hgvsp: ENSP00000437087.1:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.599G>A
  hgvsp: ENSP00000416842.2:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.599G>A
  hgvsp: ENSP00000436504.1:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.599G>A
  hgvsp: ENSP00000434501.1:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.599G>A
  hgvsp: ENSP00000345419.7:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.599G>A
  hgvsp: ENSP00000445352.1:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.599G>A
  hgvsp: ENSP00000387368.2:p.Arg200His
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.516G>A
  hgvsp: ENSP00000411558.1:p.Arg173His
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg200His
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-36168709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168709
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168709
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.610G>A
  hgvsp: ENSP00000345419.7:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.610G>A
  hgvsp: ENSP00000350267.6:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.610G>A
  hgvsp: ENSP00000436504.1:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.610G>A
  hgvsp: ENSP00000434501.1:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.610G>A
  hgvsp: ENSP00000437087.1:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.610G>A
  hgvsp: ENSP00000445352.1:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.610G>A
  hgvsp: ENSP00000387368.2:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.527G>A
  hgvsp: ENSP00000411558.1:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.610G>A
  hgvsp: ENSP00000416842.2:p.Ala204Thr
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ala204Thr
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

6-36168716-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168716
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168716
    reference: chr 6
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.617A>G
  hgvsp: ENSP00000437087.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.617A>G
  hgvsp: ENSP00000416842.2:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.617A>G
  hgvsp: ENSP00000434501.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.617A>G
  hgvsp: ENSP00000350267.6:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.534A>G
  hgvsp: ENSP00000411558.1:p.Gln179Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.617A>G
  hgvsp: ENSP00000345419.7:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.617A>G
  hgvsp: ENSP00000436504.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.617A>G
  hgvsp: ENSP00000445352.1:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.617A>G
  hgvsp: ENSP00000387368.2:p.Gln206Arg
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln206Arg
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

6-36168726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168726
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168726
    reference: chr 6
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.627C>T
  hgvsp: ENST00000532330.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.544C>T
  hgvsp: ENST00000441123.1:c.544C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.627C>T
  hgvsp: ENST00000534400.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.627C>T
  hgvsp: ENST00000534694.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.627C>T
  hgvsp: ENST00000357641.6:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.627C>T
  hgvsp: ENST00000449261.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.627C>T
  hgvsp: ENST00000543502.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.627C>T
  hgvsp: ENST00000443324.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.627C>T
  hgvsp: ENST00000339717.7:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1328
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile209Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

6-36168734-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168734
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168734
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.635A>G
  hgvsp: ENSP00000437087.1:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.635A>G
  hgvsp: ENSP00000436504.1:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.635A>G
  hgvsp: ENSP00000387368.2:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.635A>G
  hgvsp: ENSP00000434501.1:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.635A>G
  hgvsp: ENSP00000350267.6:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.635A>G
  hgvsp: ENSP00000345419.7:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.635A>G
  hgvsp: ENSP00000445352.1:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.552A>G
  hgvsp: ENSP00000411558.1:p.Asp185Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.635A>G
  hgvsp: ENSP00000416842.2:p.Asp212Gly
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp212Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-36168735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168735
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168735
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.636C>T
  hgvsp: ENST00000534694.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.636C>T
  hgvsp: ENST00000534400.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.636C>T
  hgvsp: ENST00000339717.7:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.636C>T
  hgvsp: ENST00000449261.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.636C>T
  hgvsp: ENST00000543502.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.636C>T
  hgvsp: ENST00000443324.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.636C>T
  hgvsp: ENST00000357641.6:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.553C>T
  hgvsp: ENST00000441123.1:c.553C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.636C>T
  hgvsp: ENST00000532330.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp212Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

6-36168746-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168746
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168746
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.564G>C
  hgvsp: ENSP00000411558.1:p.Cys189Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.647G>C
  hgvsp: ENSP00000345419.7:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.647G>C
  hgvsp: ENSP00000445352.1:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.647G>C
  hgvsp: ENSP00000437087.1:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.647G>C
  hgvsp: ENSP00000436504.1:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.647G>C
  hgvsp: ENSP00000387368.2:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.647G>C
  hgvsp: ENSP00000350267.6:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.647G>C
  hgvsp: ENSP00000434501.1:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.647G>C
  hgvsp: ENSP00000416842.2:p.Cys216Ser
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34002
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys216Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-36168750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168750
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168750
    reference: chr 6
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.651G>A
  hgvsp: ENST00000543502.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.651G>A
  hgvsp: ENST00000443324.2:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.651G>A
  hgvsp: ENST00000532330.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.651G>A
  hgvsp: ENST00000449261.2:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.651G>A
  hgvsp: ENST00000534400.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.568G>A
  hgvsp: ENST00000441123.1:c.568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.651G>A
  hgvsp: ENST00000357641.6:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.651G>A
  hgvsp: ENST00000339717.7:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.651G>A
  hgvsp: ENST00000534694.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val217Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

6-36168759-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168759
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168759
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.660T>A
  hgvsp: ENSP00000387368.2:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.660T>A
  hgvsp: ENSP00000345419.7:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.660T>A
  hgvsp: ENSP00000350267.6:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.660T>A
  hgvsp: ENSP00000416842.2:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.660T>A
  hgvsp: ENSP00000437087.1:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.577T>A
  hgvsp: ENSP00000411558.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.660T>A
  hgvsp: ENSP00000445352.1:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.660T>A
  hgvsp: ENSP00000434501.1:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.660T>A
  hgvsp: ENSP00000436504.1:p.Asp220Glu
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17778
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp220Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-36168772-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168772
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168772
    reference: chr 6
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.673A>G
  hgvsp: ENSP00000434501.1:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.673A>G
  hgvsp: ENSP00000387368.2:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.673A>G
  hgvsp: ENSP00000416842.2:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.673A>G
  hgvsp: ENSP00000437087.1:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.673A>G
  hgvsp: ENSP00000445352.1:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.673A>G
  hgvsp: ENSP00000345419.7:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.673A>G
  hgvsp: ENSP00000350267.6:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.590A>G
  hgvsp: ENSP00000411558.1:p.Asn198Asp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.673A>G
  hgvsp: ENSP00000436504.1:p.Asn225Asp
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn225Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

6-36168776-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168776
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168776
    reference: chr 6
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.677G>A
  hgvsp: ENSP00000445352.1:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.677G>A
  hgvsp: ENSP00000416842.2:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.677G>A
  hgvsp: ENSP00000350267.6:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.677G>A
  hgvsp: ENSP00000434501.1:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.594G>A
  hgvsp: ENSP00000411558.1:p.Ser199Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.677G>A
  hgvsp: ENSP00000345419.7:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.677G>A
  hgvsp: ENSP00000437087.1:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.677G>A
  hgvsp: ENSP00000436504.1:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.677G>A
  hgvsp: ENSP00000387368.2:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  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: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser226Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-36168792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168792
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168792
    reference: chr 6
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.693C>T
  hgvsp: ENST00000443324.2:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.610C>T
  hgvsp: ENST00000441123.1:c.610C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.693C>T
  hgvsp: ENST00000449261.2:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.693C>T
  hgvsp: ENST00000543502.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.693C>T
  hgvsp: ENST00000532330.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.693C>T
  hgvsp: ENST00000357641.6:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.693C>T
  hgvsp: ENST00000339717.7:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.693C>T
  hgvsp: ENST00000534400.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.693C>T
  hgvsp: ENST00000534694.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe231Phe
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

6-36168802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168802
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168802
    reference: chr 6
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.703T>C
  hgvsp: ENSP00000437087.1:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.703T>C
  hgvsp: ENSP00000387368.2:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.620T>C
  hgvsp: ENSP00000411558.1:p.Cys208Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.703T>C
  hgvsp: ENSP00000434501.1:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.703T>C
  hgvsp: ENSP00000416842.2:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.703T>C
  hgvsp: ENSP00000350267.6:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.703T>C
  hgvsp: ENSP00000445352.1:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.703T>C
  hgvsp: ENSP00000436504.1:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.703T>C
  hgvsp: ENSP00000345419.7:p.Cys235Arg
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys235Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-36168810-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168810
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168810
    reference: chr 6
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.711G>A
  hgvsp: ENST00000534400.1:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.711G>A
  hgvsp: ENST00000532330.1:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.711G>A
  hgvsp: ENST00000357641.6:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.711G>A
  hgvsp: ENST00000543502.1:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.711G>A
  hgvsp: ENST00000534694.1:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.711G>A
  hgvsp: ENST00000339717.7:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.711G>A
  hgvsp: ENST00000443324.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.711G>A
  hgvsp: ENST00000449261.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.628G>A
  hgvsp: ENST00000441123.1:c.628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8239
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu237Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-36168819-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168819
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168819
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.720C>T
  hgvsp: ENST00000357641.6:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.720C>T
  hgvsp: ENST00000534400.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.720C>T
  hgvsp: ENST00000532330.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.720C>T
  hgvsp: ENST00000339717.7:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.720C>T
  hgvsp: ENST00000449261.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.637C>T
  hgvsp: ENST00000441123.1:c.637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.720C>T
  hgvsp: ENST00000543502.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.720C>T
  hgvsp: ENST00000534694.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.720C>T
  hgvsp: ENST00000443324.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His240His
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

6-36168823-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168823
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168823
    reference: chr 6
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.724G>C
  hgvsp: ENSP00000434501.1:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.724G>C
  hgvsp: ENSP00000437087.1:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.724G>C
  hgvsp: ENSP00000387368.2:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.724G>C
  hgvsp: ENSP00000345419.7:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.724G>C
  hgvsp: ENSP00000350267.6:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.724G>C
  hgvsp: ENSP00000445352.1:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.724G>C
  hgvsp: ENSP00000436504.1:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.724G>C
  hgvsp: ENSP00000416842.2:p.Glu242Gln
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.641G>C
  hgvsp: ENSP00000411558.1:p.Glu215Gln
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu242Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-36168835-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168835
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168835
    reference: chr 6
allele count: 28
allele frequency: 2.306349049454713e-4
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.736G>A
  hgvsp: ENSP00000437087.1:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.736G>A
  hgvsp: ENSP00000345419.7:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.653G>A
  hgvsp: ENSP00000411558.1:p.Val219Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.736G>A
  hgvsp: ENSP00000416842.2:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.736G>A
  hgvsp: ENSP00000350267.6:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.736G>A
  hgvsp: ENSP00000436504.1:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.736G>A
  hgvsp: ENSP00000445352.1:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.736G>A
  hgvsp: ENSP00000387368.2:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.736G>A
  hgvsp: ENSP00000434501.1:p.Val246Ile
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val246Ile
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

6-36168838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168838
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168838
    reference: chr 6
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.739C>T
  hgvsp: ENSP00000445352.1:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.739C>T
  hgvsp: ENSP00000437087.1:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.739C>T
  hgvsp: ENSP00000350267.6:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.739C>T
  hgvsp: ENSP00000345419.7:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.656C>T
  hgvsp: ENSP00000411558.1:p.Pro220Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.739C>T
  hgvsp: ENSP00000434501.1:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.739C>T
  hgvsp: ENSP00000387368.2:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.739C>T
  hgvsp: ENSP00000436504.1:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.739C>T
  hgvsp: ENSP00000416842.2:p.Pro247Ser
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro247Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

6-36168855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168855
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168855
    reference: chr 6
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.756C>T
  hgvsp: ENST00000339717.7:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.673C>T
  hgvsp: ENST00000441123.1:c.673C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.756C>T
  hgvsp: ENST00000443324.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.756C>T
  hgvsp: ENST00000357641.6:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.756C>T
  hgvsp: ENST00000532330.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.756C>T
  hgvsp: ENST00000449261.2:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.756C>T
  hgvsp: ENST00000543502.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.756C>T
  hgvsp: ENST00000534694.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.756C>T
  hgvsp: ENST00000534400.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly252Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

6-36168858-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168858
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168858
    reference: chr 6
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.759G>A
  hgvsp: ENST00000532330.1:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.759G>A
  hgvsp: ENST00000543502.1:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.759G>A
  hgvsp: ENST00000443324.2:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.759G>A
  hgvsp: ENST00000449261.2:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.759G>A
  hgvsp: ENST00000534694.1:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.759G>A
  hgvsp: ENST00000357641.6:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.759G>A
  hgvsp: ENST00000534400.1:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.676G>A
  hgvsp: ENST00000441123.1:c.676G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.759G>A
  hgvsp: ENST00000339717.7:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln253Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

6-36168862-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168862
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168862
    reference: chr 6
allele count: 4
allele frequency: 3.295055768818887e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.763C>G
  hgvsp: ENSP00000437087.1:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.763C>G
  hgvsp: ENSP00000416842.2:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.763C>G
  hgvsp: ENSP00000445352.1:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.763C>G
  hgvsp: ENSP00000387368.2:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.763C>G
  hgvsp: ENSP00000434501.1:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.763C>G
  hgvsp: ENSP00000350267.6:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.680C>G
  hgvsp: ENSP00000411558.1:p.Leu228Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.763C>G
  hgvsp: ENSP00000436504.1:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.763C>G
  hgvsp: ENSP00000345419.7:p.Leu255Val
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu255Val
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

6-36168881-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168881
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168881
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.782A>G
  hgvsp: ENSP00000436504.1:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.782A>G
  hgvsp: ENSP00000345419.7:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.699A>G
  hgvsp: ENSP00000411558.1:p.Gln234Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.782A>G
  hgvsp: ENSP00000437087.1:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.782A>G
  hgvsp: ENSP00000445352.1:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.782A>G
  hgvsp: ENSP00000434501.1:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.782A>G
  hgvsp: ENSP00000350267.6:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.782A>G
  hgvsp: ENSP00000387368.2:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.782A>G
  hgvsp: ENSP00000416842.2:p.Gln261Arg
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43436
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln261Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-36168889-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168889
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168889
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.790T>A
  hgvsp: ENSP00000436504.1:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.790T>A
  hgvsp: ENSP00000437087.1:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.790T>A
  hgvsp: ENSP00000416842.2:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.790T>A
  hgvsp: ENSP00000445352.1:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.790T>A
  hgvsp: ENSP00000387368.2:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.707T>A
  hgvsp: ENSP00000411558.1:p.Ser237Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.790T>A
  hgvsp: ENSP00000434501.1:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.790T>A
  hgvsp: ENSP00000345419.7:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.790T>A
  hgvsp: ENSP00000350267.6:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2706
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8197
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser264Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

6-36168892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168892
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168892
    reference: chr 6
allele count: 6
allele frequency: 4.943479550472926e-5
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.793C>T
  hgvsp: ENSP00000434501.1:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.793C>T
  hgvsp: ENSP00000436504.1:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.793C>T
  hgvsp: ENSP00000445352.1:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.793C>T
  hgvsp: ENSP00000350267.6:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.710C>T
  hgvsp: ENSP00000411558.1:p.Arg238Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.793C>T
  hgvsp: ENSP00000345419.7:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.793C>T
  hgvsp: ENSP00000387368.2:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.793C>T
  hgvsp: ENSP00000416842.2:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.793C>T
  hgvsp: ENSP00000437087.1:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg265Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-36168894-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168894
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168894
    reference: chr 6
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.795G>A
  hgvsp: ENST00000443324.2:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.795G>A
  hgvsp: ENST00000534400.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.795G>A
  hgvsp: ENST00000543502.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.795G>A
  hgvsp: ENST00000532330.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.795G>A
  hgvsp: ENST00000357641.6:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.795G>A
  hgvsp: ENST00000449261.2:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.795G>A
  hgvsp: ENST00000339717.7:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.795G>A
  hgvsp: ENST00000534694.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.712G>A
  hgvsp: ENST00000441123.1:c.712G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg265Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

6-36168896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168896
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168896
    reference: chr 6
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.797C>T
  hgvsp: ENSP00000445352.1:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.797C>T
  hgvsp: ENSP00000345419.7:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.797C>T
  hgvsp: ENSP00000437087.1:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.797C>T
  hgvsp: ENSP00000387368.2:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.797C>T
  hgvsp: ENSP00000416842.2:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.714C>T
  hgvsp: ENSP00000411558.1:p.Pro239Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.797C>T
  hgvsp: ENSP00000350267.6:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.797C>T
  hgvsp: ENSP00000436504.1:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.797C>T
  hgvsp: ENSP00000434501.1:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro266Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

6-36168920-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168920
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168920
    reference: chr 6
allele count: 3
allele frequency: 2.472350876036327e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.821A>G
  hgvsp: ENSP00000436504.1:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.821A>G
  hgvsp: ENSP00000445352.1:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.821A>G
  hgvsp: ENSP00000350267.6:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.821A>G
  hgvsp: ENSP00000345419.7:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.738A>G
  hgvsp: ENSP00000411558.1:p.Asn247Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.821A>G
  hgvsp: ENSP00000434501.1:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.821A>G
  hgvsp: ENSP00000437087.1:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.821A>G
  hgvsp: ENSP00000387368.2:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.821A>G
  hgvsp: ENSP00000416842.2:p.Asn274Ser
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn274Ser
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

6-36168930-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168930
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168930
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.831C>T
  hgvsp: ENST00000357641.6:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.831C>T
  hgvsp: ENST00000339717.7:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.831C>T
  hgvsp: ENST00000449261.2:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.831C>T
  hgvsp: ENST00000532330.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.831C>T
  hgvsp: ENST00000534694.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.748C>T
  hgvsp: ENST00000441123.1:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.831C>T
  hgvsp: ENST00000543502.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.831C>T
  hgvsp: ENST00000534400.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.831C>T
  hgvsp: ENST00000443324.2:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly277Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

6-36168946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168946
    reference: chr 6
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.764A>G
  hgvsp: ENSP00000411558.1:p.Ser256Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.847A>G
  hgvsp: ENSP00000434501.1:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.847A>G
  hgvsp: ENSP00000437087.1:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.847A>G
  hgvsp: ENSP00000387368.2:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.847A>G
  hgvsp: ENSP00000350267.6:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.847A>G
  hgvsp: ENSP00000436504.1:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.847A>G
  hgvsp: ENSP00000345419.7:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.847A>G
  hgvsp: ENSP00000416842.2:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.847A>G
  hgvsp: ENSP00000445352.1:p.Ser283Gly
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser283Gly
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/6-36168950-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168950
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168950
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.851A>C
  hgvsp: ENSP00000387368.2:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.851A>C
  hgvsp: ENSP00000416842.2:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.851A>C
  hgvsp: ENSP00000434501.1:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.768A>C
  hgvsp: ENSP00000411558.1:p.Asp257Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.851A>C
  hgvsp: ENSP00000445352.1:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.851A>C
  hgvsp: ENSP00000437087.1:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.851A>C
  hgvsp: ENSP00000345419.7:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.851A>C
  hgvsp: ENSP00000436504.1:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.851A>C
  hgvsp: ENSP00000350267.6:p.Asp284Ala
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp284Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

6-36168954-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168954
    reference: chr 6
allele count: 291
allele frequency: 2.398615232443126e-3
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.855G>A
  hgvsp: ENST00000534694.1:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.855G>A
  hgvsp: ENST00000532330.1:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.855G>A
  hgvsp: ENST00000357641.6:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.855G>A
  hgvsp: ENST00000534400.1:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.855G>A
  hgvsp: ENST00000543502.1:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.855G>A
  hgvsp: ENST00000443324.2:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.855G>A
  hgvsp: ENST00000339717.7:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.855G>A
  hgvsp: ENST00000449261.2:c.855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.772G>A
  hgvsp: ENST00000441123.1:c.772G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17658
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 33453
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 8124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly285Gly
num of homozygotes: 6
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-36168956-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168956
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168956
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.857A>T
  hgvsp: ENSP00000350267.6:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.857A>T
  hgvsp: ENSP00000387368.2:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.857A>T
  hgvsp: ENSP00000445352.1:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.857A>T
  hgvsp: ENSP00000416842.2:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.857A>T
  hgvsp: ENSP00000434501.1:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.774A>T
  hgvsp: ENSP00000411558.1:p.His259Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.857A>T
  hgvsp: ENSP00000437087.1:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.857A>T
  hgvsp: ENSP00000436504.1:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.857A>T
  hgvsp: ENSP00000345419.7:p.His286Leu
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43101
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8176
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His286Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

6-36168979-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36168979
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36168979
    reference: chr 6
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.880A>G
  hgvsp: ENSP00000387368.2:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.880A>G
  hgvsp: ENSP00000350267.6:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.880A>G
  hgvsp: ENSP00000437087.1:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.880A>G
  hgvsp: ENSP00000416842.2:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.880A>G
  hgvsp: ENSP00000445352.1:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.880A>G
  hgvsp: ENSP00000436504.1:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.880A>G
  hgvsp: ENSP00000434501.1:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.880A>G
  hgvsp: ENSP00000345419.7:p.Ile294Val
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.797A>G
  hgvsp: ENSP00000411558.1:p.Ile267Val
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8211
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile294Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-36169005-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36169005
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36169005
    reference: chr 6
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.906T>G
  hgvsp: ENST00000443324.2:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.906T>G
  hgvsp: ENST00000534694.1:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.906T>G
  hgvsp: ENST00000357641.6:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.906T>G
  hgvsp: ENST00000543502.1:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.906T>G
  hgvsp: ENST00000534400.1:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.906T>G
  hgvsp: ENST00000532330.1:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.906T>G
  hgvsp: ENST00000449261.2:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.906T>G
  hgvsp: ENST00000339717.7:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.823T>G
  hgvsp: ENST00000441123.1:c.823T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala302Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

6-36169011-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 36169011
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 36169011
    reference: chr 6
allele count: 3
allele frequency: 2.472513887286333e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000416842
  ensembl transcript: ENST00000449261
  gene symbol: BRPF3
  hgvsc: ENST00000449261.2:c.912C>T
  hgvsp: ENST00000449261.2:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000434501
  ensembl transcript: ENST00000534694
  gene symbol: BRPF3
  hgvsc: ENST00000534694.1:c.912C>T
  hgvsp: ENST00000534694.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000437087
  ensembl transcript: ENST00000532330
  gene symbol: BRPF3
  hgvsc: ENST00000532330.1:c.912C>T
  hgvsp: ENST00000532330.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000411558
  ensembl transcript: ENST00000441123
  gene symbol: BRPF3
  hgvsc: ENST00000441123.1:c.829C>T
  hgvsp: ENST00000441123.1:c.829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000350267
  ensembl transcript: ENST00000357641
  gene symbol: BRPF3
  hgvsc: ENST00000357641.6:c.912C>T
  hgvsp: ENST00000357641.6:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000445352
  ensembl transcript: ENST00000543502
  gene symbol: BRPF3
  hgvsc: ENST00000543502.1:c.912C>T
  hgvsp: ENST00000543502.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000345419
  ensembl transcript: ENST00000339717
  gene symbol: BRPF3
  hgvsc: ENST00000339717.7:c.912C>T
  hgvsp: ENST00000339717.7:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000436504
  ensembl transcript: ENST00000534400
  gene symbol: BRPF3
  hgvsc: ENST00000534400.1:c.912C>T
  hgvsp: ENST00000534400.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000096070
  ensembl protein: ENSP00000387368
  ensembl transcript: ENST00000443324
  gene symbol: BRPF3
  hgvsc: ENST00000443324.2:c.912C>T
  hgvsp: ENST00000443324.2:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14256
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 1
hgvs: p.Thr304Thr
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 613
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43580
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.648e0

DP
type: SiteQuality
SIO_000300: 1.478947e6

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

FS
type: SiteQuality
SIO_000300: 9.041e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7746
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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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

South Asian
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allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.11e-1

MQRankSum
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DP
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SIO_000300: 1.478938e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.226e0

VQSLOD
type: SiteQuality
SIO_000300: -1.153e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e-1

QD
type: SiteQuality
SIO_000300: 1.624e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 44

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele count: 6
allele frequency: 5.193006750908776e-4
allele num: 11554
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 35
allele frequency: 5.258097470103961e-4
allele num: 66564
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.940240589833139e-4
allele num: 10308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.981e0

DP
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SIO_000300: 1.483095e6

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 5.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

QD
type: SiteQuality
SIO_000300: 1.236e1

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: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 2
allele frequency: 3.005259203606311e-5
allele num: 66550
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.572e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.916e-1

QD
type: SiteQuality
SIO_000300: 8.93e0

FS
type: SiteQuality
SIO_000300: 2.689e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
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SIO_000300: -2.829e0

DP
type: SiteQuality
SIO_000300: 1.4794e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5092439500977e-5
allele num: 66530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.556e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

FS
type: SiteQuality
SIO_000300: 1.1616e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.005e0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

BaseQRankSum
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SIO_000300: -1.935e0

QD
type: SiteQuality
SIO_000300: 1.234e1

DP
type: SiteQuality
SIO_000300: 1.479539e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.913e1

GenotypeQuality
all individuals: 613
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.961e0

VQSLOD
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SIO_000300: 4.17e-1

MQ
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SIO_000300: 5.979e1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQRankSum
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QD
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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SIO_000300: 1.479862e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.820388349514563e-4
allele num: 16480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
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: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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VQSLOD
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MQ
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QD
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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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
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: 11550
num of homozygotes: 0

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

South Asian
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QD
type: SiteQuality
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ClippingRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 617
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variant carriers: 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: 66576
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 2
allele frequency: 1.213150551983501e-4
allele num: 16486
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.368e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.481494e6

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

FS
type: SiteQuality
SIO_000300: 6.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.847e0

GenotypeQuality
all individuals: 2383
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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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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 2595
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 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: 66598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.05e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 4.994e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.482494e6

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
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: 2
allele frequency: 1.935733643050716e-4
allele num: 10332
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 1.482694e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

GenotypeQuality
all individuals: 1164
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1403
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GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 1.482965e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.513e0

QD
type: SiteQuality
SIO_000300: 1.299e1

FS
type: SiteQuality
SIO_000300: 3.519e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.65051165861417e-4
allele num: 66646
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
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: 6
allele frequency: 5.186721991701245e-4
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 126
allele frequency: 1.21786197564276e-2
allele num: 10346
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.685e0

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

QD
type: SiteQuality
SIO_000300: 1.349e1

DP
type: SiteQuality
SIO_000300: 1.492322e6

FS
type: SiteQuality
SIO_000300: 5.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10352
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
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: 16496
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 3.735e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.365e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

DP
type: SiteQuality
SIO_000300: 1.485376e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 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: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.485514e6

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.1e-1

FS
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.62e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 620
bin: 9.25e1
variant carriers: 0

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

African
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: 904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.762e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.109e0

DP
type: SiteQuality
SIO_000300: 1.485691e6

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.241910071506484e-4
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997541008186643e-5
allele num: 66694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.658e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.02e-1

DP
type: SiteQuality
SIO_000300: 1.488115e6

QD
type: SiteQuality
SIO_000300: 1.252e1

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

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2397
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 66706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.0139e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.182e1

DP
type: SiteQuality
SIO_000300: 1.488168e6

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.829e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
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: 6614
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.326e-1

FS
type: SiteQuality
SIO_000300: 1.901e0

MQRankSum
type: SiteQuality
SIO_000300: -6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.357e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.48945e6

QD
type: SiteQuality
SIO_000300: 1.457e1

MQ
type: SiteQuality
SIO_000300: 5.882e1

GenotypeQuality
all individuals: 7851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 510
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
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

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: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.072e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.931e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.490694e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.372e1

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.25e1
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
all individuals: 18
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2604
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variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1416
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variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 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: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
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: 10400
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

FS
type: SiteQuality
SIO_000300: 2.378e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

DP
type: SiteQuality
SIO_000300: 1.490913e6

GenotypeQuality
all individuals: 512
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2598
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 625
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variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.056201550387597e-4
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.491446e6

QD
type: SiteQuality
SIO_000300: 1.507e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.572e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

FS
type: SiteQuality
SIO_000300: 5.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.57e-1

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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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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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.055e0

DP
type: SiteQuality
SIO_000300: 1.49134e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.198e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 31
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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: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.094e1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.12e-1

DP
type: SiteQuality
SIO_000300: 1.491996e6

GenotypeQuality
all individuals: 510
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 11574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 1.492029e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

QD
type: SiteQuality
SIO_000300: 9.02e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

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

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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: 3.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 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: 11570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
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: 10400
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: -9.94e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

FS
type: SiteQuality
SIO_000300: 4.875e0

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 1.492377e6

MQRankSum
type: SiteQuality
SIO_000300: -1.024e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.78e-1

GenotypeQuality
all individuals: 1222
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 2601
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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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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 15
allele frequency: 1.733302519066328e-3
allele num: 8654
num of homozygotes: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.191e0

DP
type: SiteQuality
SIO_000300: 1.493538e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7891
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variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 8.86e-1

DP
type: SiteQuality
SIO_000300: 1.493211e6

QD
type: SiteQuality
SIO_000300: 9.720000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1028
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
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variant carriers: 2

GenotypeQuality
all individuals: 6820
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variant carriers: 1

GenotypeQuality
all individuals: 17
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variant carriers: 1

GenotypeQuality
all individuals: 2178
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variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
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GenotypeQuality
all individuals: 8227
bin: 9.75e1
variant carriers: 7312

GenotypeQuality
all individuals: 436
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variant carriers: 1

GenotypeQuality
all individuals: 39666
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 2

South Asian
type: Population
allele count: 1909
allele frequency: 1.156128875968992e-1
allele num: 16512
num of homozygotes: 139

East Asian
type: Population
allele count: 19
allele frequency: 2.195516524150682e-3
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 404
allele frequency: 3.490582339726974e-2
allele num: 11574
num of homozygotes: 7

Other
type: Population
allele count: 47
allele frequency: 5.176211453744493e-2
allele num: 908
num of homozygotes: 3

African
type: Population
allele count: 108
allele frequency: 1.038461538461538e-2
allele num: 10400
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 336
allele frequency: 5.080133051103719e-2
allele num: 6614
num of homozygotes: 9

European (Non-Finnish)
type: Population
allele count: 4845
allele frequency: 7.26190833058545e-2
allele num: 66718
num of homozygotes: 183

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.840664e6

QD
type: SiteQuality
SIO_000300: 1.481e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.031e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 5.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.96e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43450
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 8251
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variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.535491e6

FS
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 9.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.95e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.16e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 8250
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 566
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GenotypeQuality
all individuals: 1471
bin: 9.75e1
variant carriers: 1

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.185e0

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

DP
type: SiteQuality
SIO_000300: 1.535435e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.494e1

GenotypeQuality
all individuals: 2337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1338
bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
all individuals: 8248
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 504
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variant carriers: 0

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

GenotypeQuality
all individuals: 43463
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.53542e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e-1

FS
type: SiteQuality
SIO_000300: 3.062e0

QD
type: SiteQuality
SIO_000300: 1.413e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 8224
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 1332
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 25
bin: 3.25e1
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GenotypeQuality
all individuals: 2325
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 1463
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variant carriers: 1

GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2681
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GenotypeQuality
all individuals: 562
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 43425
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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FS
type: SiteQuality
SIO_000300: 4.5e-1

BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

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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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495190146543199e-5
allele num: 66738
num of homozygotes: 0

Other
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allele num: 908
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

South Asian
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allele count: 7
allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 0

Other
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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

Latino
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allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 1.109e0

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

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

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
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)
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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
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DP
type: SiteQuality
SIO_000300: 1.536037e6

BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

East Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

African
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South Asian
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

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

DP
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ClippingRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 9.62e-1

FS
type: SiteQuality
SIO_000300: 2.27e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 7.48e-1

ReadPosRankSum
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SIO_000300: 2.3e-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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bin: 8.25e1
variant carriers: 0

East Asian
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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

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

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

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
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
allele num: 16512
num of homozygotes: 0

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

African
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allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.027e0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 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
allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 1.4e0

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.364e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.536345e6

QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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QD
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DP
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FS
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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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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Other
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European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
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South Asian
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Latino
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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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MQRankSum
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DP
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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South Asian
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European (Finnish)
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African
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allele frequency: 9.609840476648087e-5
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num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.884e0

VQSLOD
type: SiteQuality
SIO_000300: -1.033e0

MQ
type: SiteQuality
SIO_000300: 5.791e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.148e0

MQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.536132e6

QD
type: SiteQuality
SIO_000300: 1.175e1

GenotypeQuality
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bin: 6.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.008e0

FS
type: SiteQuality
SIO_000300: 7.687e0

DP
type: SiteQuality
SIO_000300: 1.535913e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.792e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.441e1

GenotypeQuality
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variant carriers: 0

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

Latino
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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

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

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

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

African
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allele count: 2
allele frequency: 1.921968095329617e-4
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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: -2.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

FS
type: SiteQuality
SIO_000300: 2.071e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

DP
type: SiteQuality
SIO_000300: 1.535896e6

QD
type: SiteQuality
SIO_000300: 1.636e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-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: 22
allele frequency: 3.296769166217107e-4
allele num: 66732
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: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

DP
type: SiteQuality
SIO_000300: 1.537408e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

European (Finnish)
type: Population
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: 11578
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.174e1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 2.853e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.351e0

DP
type: SiteQuality
SIO_000300: 1.535856e6

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.994844433786943e-5
allele num: 66724
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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FS
type: SiteQuality
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
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allele count: 0
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African
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allele frequency: 0.0e0
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European (Finnish)
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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 count: 4
allele frequency: 5.994844433786943e-5
allele num: 66724
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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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: 1.534981e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 1.478e0

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 1.156e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.457e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
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

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

African
type: Population
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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
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SIO_000300: -1.658e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
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SIO_000300: 1.533939e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

QD
type: SiteQuality
SIO_000300: 1.272e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996641880546894e-5
allele num: 66704
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: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.13e-1

InbreedingCoeff
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SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.534127e6

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 43304
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.228e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.307e0

DP
type: SiteQuality
SIO_000300: 1.533468e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.972e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.338e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 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: 2
allele frequency: 2.998590662388677e-5
allele num: 66698
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

DP
type: SiteQuality
SIO_000300: 1.533273e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.248e0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 1.296e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.498560460652591e-5
allele num: 66688
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 count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.175000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.87e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

DP
type: SiteQuality
SIO_000300: 1.530915e6

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

GenotypeQuality
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variant carriers: 0

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

East Asian
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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: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

InbreedingCoeff
type: SiteQuality
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DP
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 6.0e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

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

East Asian
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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
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

Other
type: Population
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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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 1.530384e6

FS
type: SiteQuality
SIO_000300: 5.707e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.442e0

QD
type: SiteQuality
SIO_000300: 1.515e1

MQ
type: SiteQuality
SIO_000300: 5.848e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 9.75e1
variant carriers: 285

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 17
allele frequency: 1.468555632342778e-3
allele num: 11576
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: 66672
num of homozygotes: 0

African
type: Population
allele count: 272
allele frequency: 2.619414483821263e-2
allele num: 10384
num of homozygotes: 6

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

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.308e1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.91e-2

DP
type: SiteQuality
SIO_000300: 1.548807e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.509e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

DP
type: SiteQuality
SIO_000300: 1.532006e6

FS
type: SiteQuality
SIO_000300: 1.653e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

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

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
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variant carriers: 0

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

GenotypeQuality
all individuals: 43186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2310
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 8652
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.195e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.533412e6

VQSLOD
type: SiteQuality
SIO_000300: -2.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
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variant carriers: 0

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

GenotypeQuality
all individuals: 43208
bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

FS
type: SiteQuality
SIO_000300: 1.4344e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

DP
type: SiteQuality
SIO_000300: 1.534608e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.654e0

QD
type: SiteQuality
SIO_000300: 1.664e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.007e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0