7-156437338-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437338
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437338
    reference: chr 7
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.161G>A
  hgvsp: ENSP00000405588.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.49G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.161G>A
  hgvsp: ENSP00000385815.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.161G>A
  hgvsp: ENSP00000376499.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.161G>A
  hgvsp: ENSP00000315950.5:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.161G>A
  hgvsp: ENSP00000376497.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.161G>A
  hgvsp: ENSP00000385285.1:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.445G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.161G>A
  hgvsp: ENSP00000376503.2:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.161G>A
  hgvsp: ENSP00000376496.1:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.161G>A
  hgvsp: ENSP00000341185.4:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.161G>A
  hgvsp: ENSP00000308894.8:p.Arg54Lys
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg54Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

7-156437344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437344
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437344
    reference: chr 7
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.167C>T
  hgvsp: ENSP00000341185.4:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.167C>T
  hgvsp: ENSP00000405588.2:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.167C>T
  hgvsp: ENSP00000376503.2:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.167C>T
  hgvsp: ENSP00000376497.2:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.167C>T
  hgvsp: ENSP00000376496.1:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.167C>T
  hgvsp: ENSP00000315950.5:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.167C>T
  hgvsp: ENSP00000376499.2:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.167C>T
  hgvsp: ENSP00000385285.1:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.451C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.167C>T
  hgvsp: ENSP00000308894.8:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.167C>T
  hgvsp: ENSP00000385815.2:p.Thr56Ile
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.55C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr56Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

7-156437354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437354
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437354
    reference: chr 7
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.177A>G
  hgvsp: ENSP00000385285.1:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.177A>G
  hgvsp: ENSP00000376499.2:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.177A>G
  hgvsp: ENSP00000341185.4:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.177A>G
  hgvsp: ENSP00000385815.2:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.461A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.177A>G
  hgvsp: ENSP00000308894.8:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.177A>G
  hgvsp: ENSP00000376497.2:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.177A>G
  hgvsp: ENSP00000376496.1:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.65A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.177A>G
  hgvsp: ENSP00000405588.2:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.177A>G
  hgvsp: ENSP00000315950.5:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.177A>G
  hgvsp: ENSP00000376503.2:p.Ile59Met
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile59Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

7-156437357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437357
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437357
    reference: chr 7
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.180A>G
  hgvsp: ENSP00000405588.2:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.180A>G
  hgvsp: ENSP00000308894.8:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.180A>G
  hgvsp: ENSP00000376496.1:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.180A>G
  hgvsp: ENSP00000315950.5:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.180A>G
  hgvsp: ENSP00000385285.1:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.180A>G
  hgvsp: ENSP00000376503.2:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.180A>G
  hgvsp: ENSP00000376499.2:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.180A>G
  hgvsp: ENSP00000341185.4:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.180A>G
  hgvsp: ENSP00000385815.2:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.180A>G
  hgvsp: ENSP00000376497.2:p.Ile60Met
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.68A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.464A>G
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile60Met
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

7-156437363-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437363
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437363
    reference: chr 7
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.470T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.186T>C
  hgvsp: ENST00000392740.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.186T>C
  hgvsp: ENST00000311822.8:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.74T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.186T>C
  hgvsp: ENST00000432459.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.186T>C
  hgvsp: ENST00000343665.4:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.186T>C
  hgvsp: ENST00000392747.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.186T>C
  hgvsp: ENST00000405335.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.186T>C
  hgvsp: ENST00000317955.5:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.186T>C
  hgvsp: ENST00000404282.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.186T>C
  hgvsp: ENST00000392743.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.186T>C
  hgvsp: ENST00000392741.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr62Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

7-156437364-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437364
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437364
    reference: chr 7
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.187G>A
  hgvsp: ENSP00000315950.5:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.187G>A
  hgvsp: ENSP00000376503.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.187G>A
  hgvsp: ENSP00000385815.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.187G>A
  hgvsp: ENSP00000405588.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.187G>A
  hgvsp: ENSP00000376497.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.187G>A
  hgvsp: ENSP00000376499.2:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.187G>A
  hgvsp: ENSP00000308894.8:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.471G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.187G>A
  hgvsp: ENSP00000341185.4:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.187G>A
  hgvsp: ENSP00000385285.1:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.187G>A
  hgvsp: ENSP00000376496.1:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.75G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly63Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

7-156437367-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437367
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437367
    reference: chr 7
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.190C>T
  hgvsp: ENSP00000385815.2:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.190C>T
  hgvsp: ENSP00000376496.1:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.78C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.190C>T
  hgvsp: ENSP00000308894.8:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.190C>T
  hgvsp: ENSP00000405588.2:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.474C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.190C>T
  hgvsp: ENSP00000376503.2:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.190C>T
  hgvsp: ENSP00000315950.5:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.190C>T
  hgvsp: ENSP00000385285.1:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.190C>T
  hgvsp: ENSP00000376499.2:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.190C>T
  hgvsp: ENSP00000341185.4:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.190C>T
  hgvsp: ENSP00000376497.2:p.Leu64Phe
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu64Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

7-156437369-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437369
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437370
    reference: chr 7
allele count: 3
allele frequency: 2.485501242750621e-5
allele num: 120700
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.199dupA
  hgvsp: ENSP00000376496.1:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.199dupA
  hgvsp: ENSP00000315950.5:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.199dupA
  hgvsp: ENSP00000308894.8:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.199dupA
  hgvsp: ENSP00000376503.2:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.199dupA
  hgvsp: ENSP00000341185.4:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.87dupA
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.199dupA
  hgvsp: ENSP00000385285.1:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.199dupA
  hgvsp: ENSP00000405588.2:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.199dupA
  hgvsp: ENSP00000376497.2:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.483dupA
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.199dupA
  hgvsp: ENSP00000376499.2:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.199dupA
  hgvsp: ENSP00000385815.2:p.Thr67AsnfsTer17
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr67AsnfsTer17
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-156437377-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437377
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437377
    reference: chr 7
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.200C>A
  hgvsp: ENSP00000341185.4:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.200C>A
  hgvsp: ENSP00000385285.1:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.200C>A
  hgvsp: ENSP00000376503.2:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.200C>A
  hgvsp: ENSP00000376496.1:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.200C>A
  hgvsp: ENSP00000308894.8:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.200C>A
  hgvsp: ENSP00000405588.2:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.484C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.200C>A
  hgvsp: ENSP00000376499.2:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.200C>A
  hgvsp: ENSP00000376497.2:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.200C>A
  hgvsp: ENSP00000315950.5:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.200C>A
  hgvsp: ENSP00000385815.2:p.Thr67Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.88C>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr67Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-156437379-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437379
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437379
    reference: chr 7
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.202A>C
  hgvsp: ENSP00000315950.5:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.486A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.202A>C
  hgvsp: ENSP00000376503.2:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.202A>C
  hgvsp: ENSP00000405588.2:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.202A>C
  hgvsp: ENSP00000385815.2:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.202A>C
  hgvsp: ENSP00000341185.4:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.202A>C
  hgvsp: ENSP00000308894.8:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.202A>C
  hgvsp: ENSP00000376496.1:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.202A>C
  hgvsp: ENSP00000376499.2:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.202A>C
  hgvsp: ENSP00000385285.1:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.202A>C
  hgvsp: ENSP00000376497.2:p.Thr68Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.90A>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr68Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

7-156437383-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437383
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437383
    reference: chr 7
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.206A>T
  hgvsp: ENSP00000376499.2:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.206A>T
  hgvsp: ENSP00000376497.2:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.206A>T
  hgvsp: ENSP00000405588.2:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.490A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.206A>T
  hgvsp: ENSP00000385285.1:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.206A>T
  hgvsp: ENSP00000315950.5:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.206A>T
  hgvsp: ENSP00000308894.8:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.206A>T
  hgvsp: ENSP00000385815.2:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.206A>T
  hgvsp: ENSP00000376503.2:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.206A>T
  hgvsp: ENSP00000376496.1:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.206A>T
  hgvsp: ENSP00000341185.4:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.94A>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln69Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

7-156437392-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437392
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437392
    reference: chr 7
allele count: 4
allele frequency: 3.316859597333245e-5
allele num: 120596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.215A>G
  hgvsp: ENSP00000315950.5:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.215A>G
  hgvsp: ENSP00000376496.1:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.103A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.215A>G
  hgvsp: ENSP00000376499.2:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.215A>G
  hgvsp: ENSP00000385815.2:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.215A>G
  hgvsp: ENSP00000341185.4:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.215A>G
  hgvsp: ENSP00000385285.1:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.215A>G
  hgvsp: ENSP00000308894.8:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.215A>G
  hgvsp: ENSP00000405588.2:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.499A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.215A>G
  hgvsp: ENSP00000376503.2:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.215A>G
  hgvsp: ENSP00000376497.2:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Lys72Arg
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS

7-156437393-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437393
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437393
    reference: chr 7
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.216A>T
  hgvsp: ENSP00000376497.2:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.216A>T
  hgvsp: ENSP00000385815.2:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.216A>T
  hgvsp: ENSP00000405588.2:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.216A>T
  hgvsp: ENSP00000308894.8:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.500A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.216A>T
  hgvsp: ENSP00000315950.5:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.216A>T
  hgvsp: ENSP00000376496.1:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.216A>T
  hgvsp: ENSP00000376499.2:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.216A>T
  hgvsp: ENSP00000385285.1:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.104A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.216A>T
  hgvsp: ENSP00000341185.4:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.216A>T
  hgvsp: ENSP00000376503.2:p.Lys72Asn
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14873
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys72Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

7-156437402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437402
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437402
    reference: chr 7
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.225C>T
  hgvsp: ENST00000432459.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.225C>T
  hgvsp: ENST00000317955.5:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.225C>T
  hgvsp: ENST00000392740.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.225C>T
  hgvsp: ENST00000405335.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.225C>T
  hgvsp: ENST00000392741.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.113C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.509C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.225C>T
  hgvsp: ENST00000392743.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.225C>T
  hgvsp: ENST00000311822.8:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.225C>T
  hgvsp: ENST00000404282.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.225C>T
  hgvsp: ENST00000392747.2:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.225C>T
  hgvsp: ENST00000343665.4:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp75Asp
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: C
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-156437406-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437406
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437406
    reference: chr 7
allele count: 2
allele frequency: 1.6604400166044e-5
allele num: 120450
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.229G>C
  hgvsp: ENSP00000376499.2:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.229G>C
  hgvsp: ENSP00000315950.5:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.229G>C
  hgvsp: ENSP00000385815.2:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.229G>C
  hgvsp: ENSP00000376496.1:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.229G>C
  hgvsp: ENSP00000341185.4:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.229G>C
  hgvsp: ENSP00000376497.2:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.229G>C
  hgvsp: ENSP00000308894.8:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.229G>C
  hgvsp: ENSP00000405588.2:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.229G>C
  hgvsp: ENSP00000376503.2:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.513G>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.117G>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.229G>C
  hgvsp: ENSP00000385285.1:p.Glu77Gln
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu77Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

7-156437427-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437427
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437427
    reference: chr 7
allele count: 1
allele frequency: 8.340840089413805e-6
allele num: 119892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.250C>T
  hgvsp: ENSP00000376503.2:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.534C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.250C>T
  hgvsp: ENSP00000315950.5:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.250C>T
  hgvsp: ENSP00000385815.2:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.250C>T
  hgvsp: ENSP00000376499.2:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.250C>T
  hgvsp: ENSP00000308894.8:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.250C>T
  hgvsp: ENSP00000376496.1:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.250C>T
  hgvsp: ENSP00000376497.2:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.250C>T
  hgvsp: ENSP00000385285.1:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.250C>T
  hgvsp: ENSP00000405588.2:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.250C>T
  hgvsp: ENSP00000341185.4:p.Pro84Ser
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.138C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro84Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-156437432-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437432
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437432
    reference: chr 7
allele count: 8
allele frequency: 6.74980172457434e-5
allele num: 118522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.255A>C
  hgvsp: ENSP00000315950.5:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.255A>C
  hgvsp: ENSP00000385285.1:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.255A>C
  hgvsp: ENSP00000341185.4:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.255A>C
  hgvsp: ENSP00000376503.2:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.255A>C
  hgvsp: ENSP00000376496.1:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.255A>C
  hgvsp: ENSP00000385815.2:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.255A>C
  hgvsp: ENSP00000376499.2:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.255A>C
  hgvsp: ENSP00000405588.2:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.539A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.143A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.255A>C
  hgvsp: ENSP00000376497.2:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.255A>C
  hgvsp: ENSP00000308894.8:p.Lys85Asn
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys85Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

7-156437434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437434
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437434
    reference: chr 7
allele count: 1
allele frequency: 8.344877079960612e-6
allele num: 119834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.257C>T
  hgvsp: ENSP00000376496.1:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.541C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.257C>T
  hgvsp: ENSP00000315950.5:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.257C>T
  hgvsp: ENSP00000376497.2:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.257C>T
  hgvsp: ENSP00000385285.1:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.257C>T
  hgvsp: ENSP00000308894.8:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.145C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.257C>T
  hgvsp: ENSP00000376499.2:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.257C>T
  hgvsp: ENSP00000376503.2:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.257C>T
  hgvsp: ENSP00000385815.2:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.257C>T
  hgvsp: ENSP00000405588.2:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.257C>T
  hgvsp: ENSP00000341185.4:p.Pro86Leu
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro86Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

7-156437435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437435
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437435
    reference: chr 7
allele count: 2
allele frequency: 1.669337606837607e-5
allele num: 119808
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.258G>A
  hgvsp: ENST00000405335.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.258G>A
  hgvsp: ENST00000317955.5:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.542G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.146G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.258G>A
  hgvsp: ENST00000432459.2:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.258G>A
  hgvsp: ENST00000392743.2:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.258G>A
  hgvsp: ENST00000404282.2:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.258G>A
  hgvsp: ENST00000392747.2:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.258G>A
  hgvsp: ENST00000392741.2:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.258G>A
  hgvsp: ENST00000392740.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.258G>A
  hgvsp: ENST00000311822.8:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.258G>A
  hgvsp: ENST00000343665.4:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro86Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

7-156437437-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437437
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437437
    reference: chr 7
allele count: 1
allele frequency: 8.346827370916315e-6
allele num: 119806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.260C>T
  hgvsp: ENSP00000376497.2:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.260C>T
  hgvsp: ENSP00000315950.5:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.260C>T
  hgvsp: ENSP00000376503.2:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.260C>T
  hgvsp: ENSP00000376499.2:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.260C>T
  hgvsp: ENSP00000385285.1:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.260C>T
  hgvsp: ENSP00000385815.2:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.148C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.260C>T
  hgvsp: ENSP00000341185.4:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.544C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.260C>T
  hgvsp: ENSP00000376496.1:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.260C>T
  hgvsp: ENSP00000405588.2:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.260C>T
  hgvsp: ENSP00000308894.8:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro87Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-156437438-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437438
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437438
    reference: chr 7
allele count: 4
allele frequency: 3.339121143315079e-5
allele num: 119792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.261G>A
  hgvsp: ENST00000317955.5:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.261G>A
  hgvsp: ENST00000343665.4:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.261G>A
  hgvsp: ENST00000392740.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.261G>A
  hgvsp: ENST00000311822.8:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.261G>A
  hgvsp: ENST00000392747.2:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.149G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.261G>A
  hgvsp: ENST00000405335.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.261G>A
  hgvsp: ENST00000392743.2:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.261G>A
  hgvsp: ENST00000404282.2:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.261G>A
  hgvsp: ENST00000432459.2:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.261G>A
  hgvsp: ENST00000392741.2:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.545G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro87Pro
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

7-156437440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437440
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437440
    reference: chr 7
allele count: 3
allele frequency: 2.504717217426152e-5
allele num: 119774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.263C>T
  hgvsp: ENSP00000405588.2:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.263C>T
  hgvsp: ENSP00000376496.1:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.263C>T
  hgvsp: ENSP00000376503.2:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.263C>T
  hgvsp: ENSP00000315950.5:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.263C>T
  hgvsp: ENSP00000376499.2:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.263C>T
  hgvsp: ENSP00000385815.2:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.263C>T
  hgvsp: ENSP00000341185.4:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.263C>T
  hgvsp: ENSP00000376497.2:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.263C>T
  hgvsp: ENSP00000385285.1:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.263C>T
  hgvsp: ENSP00000308894.8:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.547C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.151C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro88Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

7-156437441-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437441
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437441
    reference: chr 7
allele count: 4
allele frequency: 3.341073486911344e-5
allele num: 119722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.264G>A
  hgvsp: ENST00000392740.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.264G>A
  hgvsp: ENST00000405335.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.264G>A
  hgvsp: ENST00000432459.2:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.264G>A
  hgvsp: ENST00000392747.2:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.264G>A
  hgvsp: ENST00000317955.5:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.264G>A
  hgvsp: ENST00000392743.2:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.264G>A
  hgvsp: ENST00000343665.4:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.264G>A
  hgvsp: ENST00000404282.2:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.264G>A
  hgvsp: ENST00000311822.8:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.264G>A
  hgvsp: ENST00000392741.2:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.548G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.152G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14760
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro88Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

7-156437442-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437442
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437442
    reference: chr 7
allele count: 1
allele frequency: 8.352125615969264e-6
allele num: 119730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.265T>C
  hgvsp: ENST00000311822.8:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.265T>C
  hgvsp: ENST00000392740.1:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.265T>C
  hgvsp: ENST00000404282.2:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.265T>C
  hgvsp: ENST00000432459.2:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.265T>C
  hgvsp: ENST00000392747.2:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.265T>C
  hgvsp: ENST00000405335.1:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.153T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.265T>C
  hgvsp: ENST00000392743.2:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.265T>C
  hgvsp: ENST00000317955.5:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.549T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.265T>C
  hgvsp: ENST00000343665.4:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.265T>C
  hgvsp: ENST00000392741.2:c.265T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu89Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

7-156437452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437452
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437452
    reference: chr 7
allele count: 1
allele frequency: 8.367640660039494e-6
allele num: 119508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.274+1G>A
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-156437461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437461
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437461
    reference: chr 7
allele count: 5
allele frequency: 4.191395902491366e-5
allele num: 119292
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+10C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

7-156437462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437462
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437462
    reference: chr 7
allele count: 27
allele frequency: 2.263391734428703e-4
allele num: 119290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+11G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20508
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-156437466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437466
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437466
    reference: chr 7
allele count: 2
allele frequency: 1.678528266416006e-5
allele num: 119152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+15T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+15T>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-156437468-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437468
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437468
    reference: chr 7
allele count: 1
allele frequency: 8.394050297149381e-6
allele num: 119132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+17A>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum

7-156437470-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437470
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437469
    reference: chr 7
allele count: 1
allele frequency: 8.398562166157153e-6
allele num: 119068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+20delC
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: TC
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-156437471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437471
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437471
    reference: chr 7
allele count: 3
allele frequency: 2.520457715121066e-5
allele num: 119026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+20C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

7-156437482-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437482
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437482
    reference: chr 7
allele count: 1
allele frequency: 8.439388313135065e-6
allele num: 118492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+31T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+31T>G
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

7-156437485-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437485
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437485
    reference: chr 7
allele count: 7
allele frequency: 5.91426012605823e-5
allele num: 118358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+34T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+34T>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

7-156437488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437488
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437488
    reference: chr 7
allele count: 2
allele frequency: 1.691589417416605e-5
allele num: 118232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+37G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/7-156437497-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437497
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437497
    reference: chr 7
allele count: 1
allele frequency: 8.495021917156547e-6
allele num: 117716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+46A>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8631
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

7-156437500-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156437500
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156437500
    reference: chr 7
allele count: 1
allele frequency: 8.514116404999489e-6
allele num: 117452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+49T>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-156439109-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156439109
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156439109
    reference: chr 7
allele count: 1
allele frequency: 6.889899407468652e-5
allele num: 14514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.275-39C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.275-39C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1658C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1658C>G
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

7-156439135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156439135
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156439135
    reference: chr 7
allele count: 1
allele frequency: 6.943480072212192e-5
allele num: 14402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.275-13C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.275-13C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1684C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

7-156439144-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156439144
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156439144
    reference: chr 7
allele count: 7
allele frequency: 4.876689424550648e-4
allele num: 14354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376496
  ensembl transcript: ENST00000392740
  gene symbol: RNF32
  hgvsc: ENST00000392740.1:c.275-4T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1693T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.275-4T>A
  variant of: http://identifiers.org/hgnc/17118
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.275-4T>A
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-156439168-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156439168
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156439168
    reference: chr 7
allele count: 1
allele frequency: 7.064142413111048e-5
allele num: 14156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*7C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1717C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1717C>G
  variant of: http://identifiers.org/hgnc/17118
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-156439196-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156439196
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156439196
    reference: chr 7
allele count: 8
allele frequency: 5.731480154749964e-4
allele num: 13958
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*35T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1745T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1745T>A
  variant of: http://identifiers.org/hgnc/17118
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-156439208-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156439208
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156439208
    reference: chr 7
allele count: 1
allele frequency: 7.202535292422933e-5
allele num: 13884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.162+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.558+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*47C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.274+1757C>A
  variant of: http://identifiers.org/hgnc/17118
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

7-156447227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447227
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447227
    reference: chr 7
allele count: 1
allele frequency: 8.826436943934473e-6
allele num: 113296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.394G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-43C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-43C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18214
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

7-156447238-TCTAACTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447238
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447231
    reference: chr 7
allele count: 762
allele frequency: 6.659558476516753e-3
allele num: 114422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.376_382delGAGTTAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-29_559-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-29_22-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-29_*94-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-29_275-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-29_163-23delAACTCCT
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 2.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9682
  bin: 1.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 1.75e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 25590
  bin: 2.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 6
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: TCTAACTC
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

7-156447243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447243
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447243
    reference: chr 7
allele count: 2
allele frequency: 1.763295246156016e-5
allele num: 113424
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.378G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-27C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-27C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

7-156447244-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447244
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447244
    reference: chr 7
allele count: 5
allele frequency: 4.400246413799173e-5
allele num: 113630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.377A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-26T>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29068
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

7-156447255-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447255
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447254
    reference: chr 7
allele count: 2
allele frequency: 1.711215305109689e-5
allele num: 116876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.365delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-14delC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-14delC
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11264
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: GC
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

7-156447262-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447262
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447262
    reference: chr 7
allele count: 1
allele frequency: 8.471704506946798e-6
allele num: 118040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-8T>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.359A>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33840
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.275-8T>G
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-156447263-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447263
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447263
    reference: chr 7
allele count: 1
allele frequency: 8.461525443807009e-6
allele num: 118182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*94-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.22-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.163-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.358T>A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.275-7A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.559-7A>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12216
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.275-7A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-156447276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447276
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447276
    reference: chr 7
allele count: 2
allele frequency: 1.671402306535183e-5
allele num: 119660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.281A>G
  hgvsp: ENSP00000385815.2:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.281A>G
  hgvsp: ENSP00000308894.8:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.345T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.281A>G
  hgvsp: ENSP00000376499.2:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.281A>G
  hgvsp: ENSP00000385285.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.281A>G
  hgvsp: ENSP00000341185.4:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.281A>G
  hgvsp: ENSP00000315950.5:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.565A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.281A>G
  hgvsp: ENSP00000405588.2:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.169A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.281A>G
  hgvsp: ENSP00000376497.2:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*100A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.28A>G
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys94Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-156447281-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447281
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447281
    reference: chr 7
allele count: 3
allele frequency: 2.503296006408438e-5
allele num: 119842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.286G>T
  hgvsp: ENSP00000405588.2:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.570G>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.33G>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.286G>T
  hgvsp: ENSP00000341185.4:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.286G>T
  hgvsp: ENSP00000385285.1:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.340C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.286G>T
  hgvsp: ENSP00000308894.8:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.286G>T
  hgvsp: ENSP00000376499.2:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.286G>T
  hgvsp: ENSP00000315950.5:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*105G>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.286G>T
  hgvsp: ENSP00000376497.2:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.174G>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.286G>T
  hgvsp: ENSP00000385815.2:p.Gly96Cys
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly96Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

7-156447285-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447285
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447285
    reference: chr 7
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.336A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.290T>C
  hgvsp: ENSP00000376499.2:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.290T>C
  hgvsp: ENSP00000385285.1:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.37T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.290T>C
  hgvsp: ENSP00000341185.4:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.290T>C
  hgvsp: ENSP00000308894.8:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.290T>C
  hgvsp: ENSP00000405588.2:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*109T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.290T>C
  hgvsp: ENSP00000315950.5:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.178T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.290T>C
  hgvsp: ENSP00000376497.2:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.290T>C
  hgvsp: ENSP00000385815.2:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.574T>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu97Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-156447286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447286
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447286
    reference: chr 7
allele count: 2
allele frequency: 1.663755095249979e-5
allele num: 120210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.291C>T
  hgvsp: ENST00000392741.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.179C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.291C>T
  hgvsp: ENST00000392743.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*110C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.335G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.291C>T
  hgvsp: ENST00000343665.4:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.291C>T
  hgvsp: ENST00000317955.5:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.291C>T
  hgvsp: ENST00000405335.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.291C>T
  hgvsp: ENST00000311822.8:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.38C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.575C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.291C>T
  hgvsp: ENST00000432459.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.291C>T
  hgvsp: ENST00000404282.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu97Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

7-156447287-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447287
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447287
    reference: chr 7
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.292A>T
  hgvsp: ENSP00000385815.2:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.292A>T
  hgvsp: ENSP00000341185.4:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.292A>T
  hgvsp: ENSP00000315950.5:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.292A>T
  hgvsp: ENSP00000385285.1:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.292A>T
  hgvsp: ENSP00000376497.2:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.334T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.39A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.576A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.292A>T
  hgvsp: ENSP00000308894.8:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*111A>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.292A>T
  hgvsp: ENSP00000376499.2:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.292A>T
  hgvsp: ENSP00000405588.2:p.Ile98Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.180A>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile98Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

7-156447288-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447288
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447288
    reference: chr 7
allele count: 80
allele frequency: 6.64772066277775e-4
allele num: 120342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.293T>A
  hgvsp: ENSP00000385815.2:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.577T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.293T>A
  hgvsp: ENSP00000315950.5:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.293T>A
  hgvsp: ENSP00000376497.2:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.293T>A
  hgvsp: ENSP00000376499.2:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.293T>A
  hgvsp: ENSP00000341185.4:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.293T>A
  hgvsp: ENSP00000385285.1:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.293T>A
  hgvsp: ENSP00000308894.8:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.293T>A
  hgvsp: ENSP00000405588.2:p.Ile98Asn
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.333A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.181T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.40T>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*112T>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33944
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile98Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

7-156447288-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447288
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447288
    reference: chr 7
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*112T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.293T>C
  hgvsp: ENSP00000385815.2:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.293T>C
  hgvsp: ENSP00000405588.2:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.293T>C
  hgvsp: ENSP00000385285.1:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.40T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.333A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.293T>C
  hgvsp: ENSP00000376499.2:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.293T>C
  hgvsp: ENSP00000308894.8:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.293T>C
  hgvsp: ENSP00000341185.4:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.293T>C
  hgvsp: ENSP00000315950.5:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.293T>C
  hgvsp: ENSP00000376497.2:p.Ile98Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.577T>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.181T>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile98Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-156447293-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447293
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447293
    reference: chr 7
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.298C>A
  hgvsp: ENSP00000308894.8:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.298C>A
  hgvsp: ENSP00000385285.1:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.186C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.45C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.298C>A
  hgvsp: ENSP00000405588.2:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.298C>A
  hgvsp: ENSP00000376497.2:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.328G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.298C>A
  hgvsp: ENSP00000341185.4:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.298C>A
  hgvsp: ENSP00000315950.5:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.582C>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.298C>A
  hgvsp: ENSP00000385815.2:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.298C>A
  hgvsp: ENSP00000376499.2:p.Pro100Thr
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*117C>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro100Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

7-156447307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447307
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447307
    reference: chr 7
allele count: 1
allele frequency: 8.264326209484141e-6
allele num: 121002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.312A>G
  hgvsp: ENST00000392743.2:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.59A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.200A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.312A>G
  hgvsp: ENST00000405335.1:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*131A>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.312A>G
  hgvsp: ENST00000343665.4:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.312A>G
  hgvsp: ENST00000404282.2:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.312A>G
  hgvsp: ENST00000317955.5:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.312A>G
  hgvsp: ENST00000311822.8:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.312A>G
  hgvsp: ENST00000392741.2:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.312A>G
  hgvsp: ENST00000432459.2:c.312A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.314T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.596A>G
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro104Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-156447325-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447325
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447325
    reference: chr 7
allele count: 62
allele frequency: 5.113149040047503e-4
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.330G>C
  hgvsp: ENSP00000385815.2:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.330G>C
  hgvsp: ENSP00000341185.4:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.330G>C
  hgvsp: ENSP00000308894.8:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.614G>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.330G>C
  hgvsp: ENSP00000315950.5:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.330G>C
  hgvsp: ENSP00000376497.2:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.296C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.330G>C
  hgvsp: ENSP00000385285.1:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.330G>C
  hgvsp: ENSP00000405588.2:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*149G>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.77G>C
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.330G>C
  hgvsp: ENSP00000376499.2:p.Trp110Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.218G>C
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16000
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Trp110Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

7-156447338-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447338
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447338
    reference: chr 7
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.343C>G
  hgvsp: ENSP00000405588.2:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.343C>G
  hgvsp: ENSP00000385815.2:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.343C>G
  hgvsp: ENSP00000308894.8:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.283G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.343C>G
  hgvsp: ENSP00000341185.4:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.343C>G
  hgvsp: ENSP00000315950.5:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*162C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.343C>G
  hgvsp: ENSP00000385285.1:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+7C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.627C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.343C>G
  hgvsp: ENSP00000376497.2:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.343C>G
  hgvsp: ENSP00000376499.2:p.Gln115Glu
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.231C>G
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln115Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

7-156447341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447341
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447341
    reference: chr 7
allele count: 5
allele frequency: 4.119498409873614e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.280G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.630C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.346C>T
  hgvsp: ENSP00000315950.5:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.346C>T
  hgvsp: ENSP00000385815.2:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.346C>T
  hgvsp: ENSP00000376499.2:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.346C>T
  hgvsp: ENSP00000385285.1:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*165C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.346C>T
  hgvsp: ENSP00000341185.4:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.234C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+10C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.346C>T
  hgvsp: ENSP00000376497.2:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.346C>T
  hgvsp: ENSP00000308894.8:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.346C>T
  hgvsp: ENSP00000405588.2:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg116Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

7-156447342-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447342
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447342
    reference: chr 7
allele count: 11
allele frequency: 9.062000560196398e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.347G>A
  hgvsp: ENSP00000385285.1:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.279C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.631G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.347G>A
  hgvsp: ENSP00000376497.2:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.347G>A
  hgvsp: ENSP00000308894.8:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.347G>A
  hgvsp: ENSP00000341185.4:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.347G>A
  hgvsp: ENSP00000376499.2:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.347G>A
  hgvsp: ENSP00000315950.5:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.347G>A
  hgvsp: ENSP00000385815.2:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*166G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.347G>A
  hgvsp: ENSP00000405588.2:p.Arg116His
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.235G>A
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+11G>A
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg116His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-156447342-G-GCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447342
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447344
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: GCT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.353_354dupTC
  hgvsp: ENSP00000308894.8:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.353_354dupTC
  hgvsp: ENSP00000315950.5:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.353_354dupTC
  hgvsp: ENSP00000376499.2:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.353_354dupTC
  hgvsp: ENSP00000385815.2:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.277_278dupAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+17_83+18dupTC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.353_354dupTC
  hgvsp: ENSP00000376497.2:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.353_354dupTC
  hgvsp: ENSP00000341185.4:p.Leu119SerfsTer36
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.353_354dupTC
  hgvsp: ENSP00000405588.2:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.353_354dupTC
  hgvsp: ENSP00000385285.1:p.Leu119SerfsTer60
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.241_242dupTC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.637_638dupTC
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*172_*173dupTC
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu119SerfsTer60
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-156447343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447343
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447343
    reference: chr 7
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.348C>T
  hgvsp: ENST00000404282.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.632C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.348C>T
  hgvsp: ENST00000432459.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*167C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.348C>T
  hgvsp: ENST00000392743.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+12C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.278G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.236C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.348C>T
  hgvsp: ENST00000405335.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.348C>T
  hgvsp: ENST00000317955.5:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.348C>T
  hgvsp: ENST00000343665.4:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.348C>T
  hgvsp: ENST00000392741.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.348C>T
  hgvsp: ENST00000311822.8:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg116Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

7-156447345-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447345
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447345
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*169C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.350C>G
  hgvsp: ENSP00000315950.5:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.634C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.238C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.350C>G
  hgvsp: ENSP00000376497.2:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.276G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.350C>G
  hgvsp: ENSP00000405588.2:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.350C>G
  hgvsp: ENSP00000341185.4:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+14C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.350C>G
  hgvsp: ENSP00000376499.2:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.350C>G
  hgvsp: ENSP00000385815.2:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.350C>G
  hgvsp: ENSP00000308894.8:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.350C>G
  hgvsp: ENSP00000385285.1:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser117Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

7-156447347-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447347
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447347
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.352C>G
  hgvsp: ENSP00000376497.2:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.352C>G
  hgvsp: ENSP00000385815.2:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*171C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.274G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.636C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+16C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.352C>G
  hgvsp: ENSP00000376499.2:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.352C>G
  hgvsp: ENSP00000341185.4:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.352C>G
  hgvsp: ENSP00000405588.2:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.352C>G
  hgvsp: ENSP00000308894.8:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.240C>G
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.352C>G
  hgvsp: ENSP00000385285.1:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.352C>G
  hgvsp: ENSP00000315950.5:p.Leu118Val
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu118Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

7-156447347-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 156447347
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 156447347
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000341185
  ensembl transcript: ENST00000343665
  gene symbol: RNF32
  hgvsc: ENST00000343665.4:c.352C>T
  hgvsp: ENSP00000341185.4:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000472537
  gene symbol: RNF32
  hgvsc: ENST00000472537.1:n.83+16C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000405588
  ensembl transcript: ENST00000432459
  gene symbol: RNF32
  hgvsc: ENST00000432459.2:c.352C>T
  hgvsp: ENSP00000405588.2:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385285
  ensembl transcript: ENST00000405335
  gene symbol: RNF32
  hgvsc: ENST00000405335.1:c.352C>T
  hgvsp: ENSP00000385285.1:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376499
  ensembl transcript: ENST00000392743
  gene symbol: RNF32
  hgvsc: ENST00000392743.2:c.352C>T
  hgvsp: ENSP00000376499.2:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000385815
  ensembl transcript: ENST00000404282
  gene symbol: RNF32
  hgvsc: ENST00000404282.2:c.352C>T
  hgvsp: ENSP00000385815.2:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376497
  ensembl transcript: ENST00000392741
  gene symbol: RNF32
  hgvsc: ENST00000392741.2:c.352C>T
  hgvsp: ENSP00000376497.2:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000308894
  ensembl transcript: ENST00000311822
  gene symbol: RNF32
  hgvsc: ENST00000311822.8:c.352C>T
  hgvsp: ENSP00000308894.8:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000469382
  gene symbol: RNF32
  hgvsc: ENST00000469382.1:n.636C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000315950
  ensembl transcript: ENST00000317955
  gene symbol: RNF32
  hgvsc: ENST00000317955.5:c.352C>T
  hgvsp: ENSP00000315950.5:p.Leu118Phe
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105982
  ensembl transcript: ENST00000480011
  gene symbol: RNF32
  hgvsc: ENST00000480011.1:n.240C>T
  variant of: http://identifiers.org/hgnc/17118
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000224903
  ensembl transcript: ENST00000455709
  gene symbol: AC005534.8
  hgvsc: ENST00000455709.1:n.274G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000105982
  ensembl protein: ENSP00000376503
  ensembl transcript: ENST00000392747
  gene symbol: RNF32
  hgvsc: ENST00000392747.2:c.*171C>T
  variant of: http://identifiers.org/hgnc/17118
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu118Phe
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1213
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1550
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 919
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25719
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50665943470138e-5
allele num: 66372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.838e0

MQ
type: SiteQuality
SIO_000300: 3.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.352e0

QD
type: SiteQuality
SIO_000300: 1.63e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

DP
type: SiteQuality
SIO_000300: 1.874778e6

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2829
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2309
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25793
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3638
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8067
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0126e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.391e-1

QD
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SIO_000300: 1.403e1

BaseQRankSum
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SIO_000300: -1.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.876377e6

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 3.418e1

InbreedingCoeff
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SIO_000300: 1.2e-3

BaseQRankSum
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SIO_000300: -1.588e0

DP
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SIO_000300: 1.878101e6

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

FS
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SIO_000300: 1.455e1

ReadPosRankSum
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SIO_000300: -1.953e0

QD
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SIO_000300: 4.91e0

ClippingRankSum
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SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
SIO_000300: -2.209e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66342
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.164e0

VQSLOD
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SIO_000300: 8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e0

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
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SIO_000300: 5.26e0

MQRankSum
type: SiteQuality
SIO_000300: -3.71e-1

QD
type: SiteQuality
SIO_000300: 1.092e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.878594e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.185e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
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SIO_000300: -5.98e-1

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

ClippingRankSum
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SIO_000300: -5.26e-1

BaseQRankSum
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SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

DP
type: SiteQuality
SIO_000300: 1.878862e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

African
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allele count: 1
allele frequency: 9.742790335151988e-5
allele num: 10264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

Latino
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allele count: 0
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allele num: 11532
num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.919e1

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

GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50779530170984e-5
allele num: 66322
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 3.483511379470506e-4
allele num: 8612
num of homozygotes: 0

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

African
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Other
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Latino
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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Other
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African
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ReadPosRankSum
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BaseQRankSum
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

Other
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South Asian
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African
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East Asian
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European (Finnish)
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allele frequency: 3.024803387779795e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.017501508750754e-5
allele num: 66280
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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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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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

European (Finnish)
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Other
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African
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East Asian
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European (Non-Finnish)
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South Asian
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QD
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DP
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Other
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Latino
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South Asian
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VQSLOD
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QD
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MQRankSum
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 1.544640098856966e-4
allele num: 6474
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Other
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East Asian
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African
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South Asian
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European (Non-Finnish)
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allele num: 64974
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Latino
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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FS
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.098304671301378e-5
allele num: 16398
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African
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.519803033526855e-5
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DP
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SIO_000300: 1.889984e6

MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
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num of homozygotes: 0

Other
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East Asian
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South Asian
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Latino
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African
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European (Non-Finnish)
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QD
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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QD
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
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allele num: 10018
num of homozygotes: 0

Latino
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allele num: 11492
num of homozygotes: 0

Other
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South Asian
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East Asian
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allele num: 8556
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European (Non-Finnish)
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allele frequency: 1.52077376969402e-5
allele num: 65756
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQ
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 65758
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African
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East Asian
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Other
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allele frequency: 0.0e0
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European (Finnish)
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ClippingRankSum
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SIO_000300: -2.19e-1

InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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DP
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SIO_000300: 1.887768e6

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

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

South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65624
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Latino
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Other
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European (Finnish)
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BaseQRankSum
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SIO_000300: -1.498e0

MQ
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SIO_000300: 6.0e1

DP
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QD
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VQSLOD
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ReadPosRankSum
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FS
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SIO_000300: 6.944e0

MQRankSum
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SIO_000300: -6.59e-1

ClippingRankSum
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SIO_000300: 1.02e0

InbreedingCoeff
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SIO_000300: -7.0e-4

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.008471157724889e-4
allele num: 9916
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.106497313141182e-5
allele num: 16376
num of homozygotes: 0

European (Finnish)
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allele count: 1
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allele num: 6598
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Other
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East Asian
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allele num: 8520
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European (Non-Finnish)
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allele num: 65524
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

VQSLOD
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MQ
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SIO_000300: 5.989e1

InbreedingCoeff
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SIO_000300: -8.0e-4

FS
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QD
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MQRankSum
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SIO_000300: 7.61e-1

BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: 8.080000000000001e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 26

African
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allele count: 22
allele frequency: 2.21953188054883e-3
allele num: 9912
num of homozygotes: 0

Latino
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allele frequency: 1.744896178677369e-4
allele num: 11462
num of homozygotes: 0

East Asian
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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allele num: 65526
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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MQRankSum
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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East Asian
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allele num: 8512
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European (Finnish)
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Other
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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QD
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.536145503702111e-5
allele num: 65098
num of homozygotes: 0

African
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East Asian
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European (Finnish)
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Latino
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South Asian
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Other
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DP
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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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FS
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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variant carriers: 0

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

African
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num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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African
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QD
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FS
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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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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.305483028720627e-4
allele num: 7660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5012
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.60944e5

VQSLOD
type: SiteQuality
SIO_000300: -6.955e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.95e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.45e-1

FS
type: SiteQuality
SIO_000300: 1.379e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.43e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeDepth
all individuals: 342
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 2.5e0
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GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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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: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.306165099268548e-4
allele num: 7656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: -2.427e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

FS
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 2.59495e5

MQ
type: SiteQuality
SIO_000300: 5.912e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.254e0

QD
type: SiteQuality
SIO_000300: 8.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.846e0

GenotypeDepth
all individuals: 69
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14
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variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 546
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GenotypeQuality
all individuals: 704
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 7.042253521126761e-3
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.306506401881369e-4
allele num: 7654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

DP
type: SiteQuality
SIO_000300: 2.58539e5

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.17e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

GenotypeQuality
all individuals: 1503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
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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
all individuals: 222
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.072109407376709e-4
allele num: 4826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.354e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.012e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

DP
type: SiteQuality
SIO_000300: 2.54828e5

QD
type: SiteQuality
SIO_000300: 8.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.98e-1

GenotypeQuality
all individuals: 2324
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 126
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 402
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GenotypeQuality
all individuals: 373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
all individuals: 464
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 1174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.699235344095157e-3
allele num: 4708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-1

DP
type: SiteQuality
SIO_000300: 2.49539e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

FS
type: SiteQuality
SIO_000300: 4.948e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 188
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GenotypeQuality
all individuals: 747
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313370107696349e-4
allele num: 7614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.91e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.512e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

DP
type: SiteQuality
SIO_000300: 2.47309e5

QD
type: SiteQuality
SIO_000300: 1.193e1

GenotypeDepth
all individuals: 418
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variant carriers: 0

GenotypeDepth
all individuals: 927
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variant carriers: 0

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

GenotypeQuality
all individuals: 4826
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.565925461948011e-4
allele num: 6386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.267337e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

VQSLOD
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SIO_000300: 6.38e-1

BaseQRankSum
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SIO_000300: -1.448e0

MQRankSum
type: SiteQuality
SIO_000300: 8.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 24
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variant carriers: 2

GenotypeDepth
all individuals: 150
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variant carriers: 5

GenotypeDepth
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GenotypeQuality
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variant carriers: 739

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2223
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GenotypeQuality
all individuals: 24056
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 4050
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1497
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4135
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 15
allele frequency: 1.516683518705763e-3
allele num: 9890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 380
allele frequency: 6.002400960384154e-3
allele num: 63308
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 13
allele frequency: 2.026184538653367e-3
allele num: 6416
num of homozygotes: 0

Latino
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allele count: 21
allele frequency: 1.921669106881406e-3
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Other
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allele frequency: 8.254716981132075e-3
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East Asian
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allele frequency: 9.073312363900314e-3
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.184307731499172e-5
allele num: 62808
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.953424744695065e-5
allele num: 62866
num of homozygotes: 0

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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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.550339524355834e-5
allele num: 64502
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
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num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.480881399870383e-5
allele num: 15430
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 7.64e-1

QD
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DP
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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SIO_000300: 1.45e0

VQSLOD
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SIO_000300: 1.43e0

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

African
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East Asian
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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African
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Latino
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Other
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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DP
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65940
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Other
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South Asian
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Latino
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European (Finnish)
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African
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East Asian
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MQRankSum
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DP
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

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

Latino
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allele frequency: 2.638986629134412e-4
allele num: 11368
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66020
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -2.255e0

ReadPosRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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SIO_000300: -5.4e-1

MQ
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FS
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MQRankSum
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SIO_000300: 1.22e0

VQSLOD
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DP
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SIO_000300: 1.542262e6

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511624391571182e-5
allele num: 66154
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11400
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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MQRankSum
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SIO_000300: -8.22e-1

InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

QD
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FS
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VQSLOD
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BaseQRankSum
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DP
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SIO_000300: 1.551414e6

ClippingRankSum
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SIO_000300: -1.627e0

ReadPosRankSum
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SIO_000300: 1.38e0

GenotypeDepth
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variant carriers: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66188
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.948937828883259e-4
allele num: 10262
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: -2.63e-1

InbreedingCoeff
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ClippingRankSum
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FS
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MQRankSum
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BaseQRankSum
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DP
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MQ
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SIO_000300: 5.951e1

VQSLOD
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SIO_000300: 8.91e-1

QD
type: SiteQuality
SIO_000300: 1.133e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 894
num of homozygotes: 0

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

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

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

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

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

European (Finnish)
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allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

FS
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SIO_000300: 5.633e0

BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 5.941e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 15

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 80

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

African
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allele frequency: 0.0e0
allele num: 10274
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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Latino
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allele num: 11420
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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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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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66332
num of homozygotes: 0

South Asian
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East Asian
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Other
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Latino
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African
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European (Finnish)
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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FS
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeDepth
all individuals: 15633
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 255
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33456
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3569
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
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: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.387e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

DP
type: SiteQuality
SIO_000300: 1.578455e6

QD
type: SiteQuality
SIO_000300: 1.218e1

FS
type: SiteQuality
SIO_000300: 3.151e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.841e-1

GenotypeDepth
all individuals: 101
bin: 6.75e1
variant carriers: 7

GenotypeDepth
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 6.25e1
variant carriers: 8

GenotypeDepth
all individuals: 76
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 77
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7618
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 9.75e1
variant carriers: 62

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

East Asian
type: Population
allele count: 62
allele frequency: 7.167630057803468e-3
allele num: 8650
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.588924e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 1.852e0

QD
type: SiteQuality
SIO_000300: 1.336e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

GenotypeDepth
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2015
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 39102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3582
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2804
bin: 7.25e1
variant carriers: 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: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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: 11568
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: 1.589965e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 7.193e0

QD
type: SiteQuality
SIO_000300: 1.34e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

GenotypeDepth
all individuals: 428
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1022
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 95
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1057
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 867
bin: 8.75e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493330935467435e-5
allele num: 66726
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: 11570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.404e0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.224e1

MQRankSum
type: SiteQuality
SIO_000300: -3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.59045e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

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

GenotypeDepth
all individuals: 26
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39099
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3592
bin: 9.75e1
variant carriers: 11

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

GenotypeQuality
all individuals: 7675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.029201502483945e-4
allele num: 16506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.19e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

DP
type: SiteQuality
SIO_000300: 1.591082e6

GenotypeDepth
all individuals: 6344
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 151
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2017
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7675
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 867
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3592
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39099
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 9.25e1
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: 66732
num of homozygotes: 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: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.591082e6

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.19e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

GenotypeDepth
all individuals: 77
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39132
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3583
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7677
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3312
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 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: 11572
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.349e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

MQ
type: SiteQuality
SIO_000300: 5.869e1

DP
type: SiteQuality
SIO_000300: 1.590873e6

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.427e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.524e1

GenotypeDepth
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3313
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 866
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 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: 11572
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

FS
type: SiteQuality
SIO_000300: 1.968e0

DP
type: SiteQuality
SIO_000300: 1.59082e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

QD
type: SiteQuality
SIO_000300: 1.101e1

MQRankSum
type: SiteQuality
SIO_000300: -7.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.06e-1

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

GenotypeDepth
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1023
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7685
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3312
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 864
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3584
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 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

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: 8654
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: 66730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.729e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

FS
type: SiteQuality
SIO_000300: 2.061e0

QD
type: SiteQuality
SIO_000300: 1.218e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

DP
type: SiteQuality
SIO_000300: 1.590944e6