3-32746271-TTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746271
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746269
    reference: chr 3
allele count: 86
allele frequency: 7.630607609312891e-4
allele num: 112704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-17_118-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-17_298-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-17_36-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+832_117+833delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-17_-424-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-17_118-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3876_171-3875delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-17_383-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-17_173-16delTG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3876_171-3875delTG
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 3.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 1.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 1.25e1
  variant carriers: 23
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: TTG
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

3-32746271-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746271
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746271
    reference: chr 3
allele count: 1
allele frequency: 8.872799545712663e-6
allele num: 112704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+817T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3891T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-32T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-32T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-32T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-32T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3891T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-32T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-32T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-32T>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-32746285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746285
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746285
    reference: chr 3
allele count: 1
allele frequency: 8.586934121041424e-6
allele num: 116456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+831G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3877G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-18G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3877G>A
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6304
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

3-32746288-G-GAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746288
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746290
    reference: chr 3
allele count: 2
allele frequency: 2.684707903780069e-5
allele num: 74496
alternate allele: GAT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+834_117+835insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-15_36-14insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-15_-424-14insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-15_118-14insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3874_171-3873insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-15_383-14insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3874_171-3873insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-15_173-14insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-15_118-14insAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-15_298-14insAT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1929
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

3-32746288-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746288
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746289
    reference: chr 3
allele count: 10516
allele frequency: 1.41161941580756e-1
allele num: 74496
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3862dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+846dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-3dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3862dupT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 981
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 6.25e1
  variant carriers: 439
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 313
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 188
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 489
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.25e1
  variant carriers: 693
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 942
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.75e1
  variant carriers: 525
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.75e1
  variant carriers: 1615
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 1534
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 1713
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.25e1
  variant carriers: 1286
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 406
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 7.25e1
  variant carriers: 382
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.75e1
  variant carriers: 346
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 765
genotype quality: GenotypeQuality
  all individuals: 3503
  bin: 1.75e1
  variant carriers: 681
genotype quality: GenotypeQuality
  all individuals: 2756
  bin: 6.25e1
  variant carriers: 349
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 7.25e1
  variant carriers: 260
num of homozygotes: 21
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

3-32746288-G-GTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746288
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746290
    reference: chr 3
allele count: 441
allele frequency: 5.919780927835051e-3
allele num: 74496
alternate allele: GTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-4_-424-3dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-4_118-3dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-4_118-3dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-4_173-3dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+845_117+846dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3863_171-3862dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-4_36-3dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-4_383-3dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3863_171-3862dupTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-4_298-3dupTT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 1.25e1
  variant carriers: 11
num of homozygotes: 3
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

3-32746288-G-GTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746288
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746291
    reference: chr 3
allele count: 12
allele frequency: 1.610824742268041e-4
allele num: 74496
alternate allele: GTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-5_118-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-5_118-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-5_298-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-5_36-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3864_171-3862dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3864_171-3862dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-5_173-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-5_-424-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-5_383-3dupTTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+844_117+846dupTTT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 1.25e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

3-32746288-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746288
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746287
    reference: chr 3
allele count: 11010
allele frequency: 1.477931701030928e-1
allele num: 74496
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-3delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-3delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+846delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-3delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-3delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3862delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-3delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-3delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3862delT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-3delT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 1565
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 269
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.75e1
  variant carriers: 764
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 1466
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 765
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.25e1
  variant carriers: 1120
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 7.25e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 294
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 394
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 6.25e1
  variant carriers: 499
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.75e1
  variant carriers: 2398
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.25e1
  variant carriers: 2023
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 2036
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 520
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 163
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 4.25e1
  variant carriers: 749
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 7.25e1
  variant carriers: 434
genotype quality: GenotypeQuality
  all individuals: 3503
  bin: 1.75e1
  variant carriers: 1034
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: GT
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

3-32746288-GTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746288
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746286
    reference: chr 3
allele count: 64
allele frequency: 8.59106529209622e-4
allele num: 74496
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-4_36-3delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-4_383-3delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3863_171-3862delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3863_171-3862delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-4_118-3delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+845_117+846delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-4_-424-3delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-4_298-3delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-4_118-3delTT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-4_173-3delTT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4122
  bin: 7.5e0
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: GTT
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

3-32746290-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746290
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746290
    reference: chr 3
allele count: 1
allele frequency: 1.527557130636686e-5
allele num: 65464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-13T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3872T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3872T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+836T>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3226
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

3-32746295-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746295
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746295
    reference: chr 3
allele count: 52
allele frequency: 4.341799843027237e-4
allele num: 119766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-8T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-8T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+841T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3867T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-8T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-8T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-8T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-8T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3867T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-8T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23519
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
hgvs: c.298-8T>C
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

3-32746300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746300
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746300
    reference: chr 3
allele count: 2
allele frequency: 1.670201927413024e-5
allele num: 119746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.118-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.36-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3862T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.298-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-424-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.383-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.173-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.118-3T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3862T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+846T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32195
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 8.75e1
  variant carriers: 0
hgvs: c.298-3T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-32746329-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746329
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746329
    reference: chr 3
allele count: 48
allele frequency: 3.994208397823156e-4
allele num: 120174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-398A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.144A>G
  hgvsp: ENST00000328834.5:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3833A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.62A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+875A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3833A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.324A>G
  hgvsp: ENST00000454516.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.409A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.20A>G
  hgvsp: ENST00000416457.1:c.20A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.144A>G
  hgvsp: ENST00000331889.6:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.199A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15489
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24927
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gln108Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/3-32746330-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746330
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746330
    reference: chr 3
allele count: 1
allele frequency: 8.320990530712775e-6
allele num: 120178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.410C>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.325C>A
  hgvsp: ENSP00000399862.2:p.His109Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-397C>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.21C>A
  hgvsp: ENSP00000402979.1:p.His8Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.63C>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3832C>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.200C>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.145C>A
  hgvsp: ENSP00000330060.5:p.His49Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.145C>A
  hgvsp: ENSP00000329376.6:p.His49Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3832C>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+876C>A
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His109Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

3-32746337-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746337
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746337
    reference: chr 3
allele count: 1
allele frequency: 8.315040244794785e-6
allele num: 120264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.28C>G
  hgvsp: ENSP00000402979.1:p.Ala10Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3825C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.70C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.152C>G
  hgvsp: ENSP00000329376.6:p.Ala51Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.332C>G
  hgvsp: ENSP00000399862.2:p.Ala111Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.207C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.417C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3825C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-390C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+883C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.152C>G
  hgvsp: ENSP00000330060.5:p.Ala51Gly
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala111Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

3-32746340-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746340
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746340
    reference: chr 3
allele count: 1
allele frequency: 8.312413758707254e-6
allele num: 120302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.155G>C
  hgvsp: ENSP00000329376.6:p.Cys52Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+886G>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.31G>C
  hgvsp: ENSP00000402979.1:p.Cys11Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.335G>C
  hgvsp: ENSP00000399862.2:p.Cys112Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3822G>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.73G>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-387G>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.155G>C
  hgvsp: ENSP00000330060.5:p.Cys52Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.210G>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.420G>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3822G>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys112Ser
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

3-32746344-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746344
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746344
    reference: chr 3
allele count: 5
allele frequency: 4.155239757333998e-5
allele num: 120330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3818A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-383A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.424A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.77A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3818A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.159A>G
  hgvsp: ENST00000331889.6:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+890A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.35A>G
  hgvsp: ENST00000416457.1:c.35A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.159A>G
  hgvsp: ENST00000328834.5:c.159A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.339A>G
  hgvsp: ENST00000454516.2:c.339A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.214A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu113Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-32746346-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746346
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746346
    reference: chr 3
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.37A>G
  hgvsp: ENSP00000402979.1:p.Gln13Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+892A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-381A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.216A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.161A>G
  hgvsp: ENSP00000329376.6:p.Gln54Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.426A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3816A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3816A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.161A>G
  hgvsp: ENSP00000330060.5:p.Gln54Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.341A>G
  hgvsp: ENSP00000399862.2:p.Gln114Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.79A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln114Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

3-32746348-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746348
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746348
    reference: chr 3
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.428G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+894G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.39G>A
  hgvsp: ENSP00000402979.1:p.Asp14Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3814G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.218G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3814G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-379G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.343G>A
  hgvsp: ENSP00000399862.2:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.81G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.163G>A
  hgvsp: ENSP00000329376.6:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.163G>A
  hgvsp: ENSP00000330060.5:p.Asp55Asn
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp115Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

3-32746349-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746349
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746349
    reference: chr 3
allele count: 4
allele frequency: 3.323031934336889e-5
allele num: 120372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.164A>T
  hgvsp: ENSP00000330060.5:p.Asp55Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.429A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+895A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3813A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.344A>T
  hgvsp: ENSP00000399862.2:p.Asp115Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.164A>T
  hgvsp: ENSP00000329376.6:p.Asp55Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3813A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.40A>T
  hgvsp: ENSP00000402979.1:p.Asp14Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.82A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-378A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.219A>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp115Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

3-32746361-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746361
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746361
    reference: chr 3
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.176A>T
  hgvsp: ENSP00000330060.5:p.Asp59Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.356A>T
  hgvsp: ENSP00000399862.2:p.Asp119Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-366A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+907A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.94A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3801A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.52A>T
  hgvsp: ENSP00000402979.1:p.Asp18Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.441A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3801A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.176A>T
  hgvsp: ENSP00000329376.6:p.Asp59Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.231A>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp119Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

3-32746383-TACAGCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746383
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746377
    reference: chr 3
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.254_259delACAGCA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.75_80delACAGCA
  hgvsp: ENSP00000402979.1:p.Thr26_Ala27del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.199_204delACAGCA
  hgvsp: ENSP00000329376.6:p.Thr67_Ala68del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.117_122delACAGCA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.464_469delACAGCA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+930_117+935delACAGCA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.379_384delACAGCA
  hgvsp: ENSP00000399862.2:p.Thr127_Ala128del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.199_204delACAGCA
  hgvsp: ENSP00000330060.5:p.Thr67_Ala68del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-343_-338delACAGCA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr127_Ala128del
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: TACAGCA
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

3-32746387-G-GTATAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746387
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746392
    reference: chr 3
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: GTATAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.467_468insTATAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.202_203insTATAT
  hgvsp: ENSP00000330060.5:p.Ala68ValfsTer4
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.120_121insTATAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3775_171-3774insTATAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.78_79insTATAT
  hgvsp: ENSP00000402979.1:p.Ala27ValfsTer4
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.257_258insTATAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.382_383insTATAT
  hgvsp: ENSP00000399862.2:p.Ala128ValfsTer4
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.202_203insTATAT
  hgvsp: ENSP00000329376.6:p.Ala68ValfsTer4
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-340_-339insTATAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+933_117+934insTATAT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3775_171-3774insTATAT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala128ValfsTer4
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

3-32746388-C-CATTCCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746388
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746394
    reference: chr 3
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: CATTCCA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.122_123insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.384_385insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.204_205insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.259_260insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+935_117+936insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.204_205insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-338_-337insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.469_470insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.80_81insTTCCAA
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15456
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala128_Val129insPheGln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

3-32746390-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746390
    reference: chr 3
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.205G>A
  hgvsp: ENSP00000330060.5:p.Val69Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-337G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+936G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.385G>A
  hgvsp: ENSP00000399862.2:p.Val129Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3772G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.205G>A
  hgvsp: ENSP00000329376.6:p.Val69Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3772G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.470G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.260G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.81G>A
  hgvsp: ENSP00000402979.1:p.Val28Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.123G>A
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15461
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val129Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

3-32746390-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746390
    reference: chr 3
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.123G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.470G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.260G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.205G>T
  hgvsp: ENSP00000330060.5:p.Val69Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3772G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+936G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-337G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.205G>T
  hgvsp: ENSP00000329376.6:p.Val69Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.385G>T
  hgvsp: ENSP00000399862.2:p.Val129Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3772G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.81G>T
  hgvsp: ENSP00000402979.1:p.Val28Leu
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val129Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

3-32746393-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746393
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746393
    reference: chr 3
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+939G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.388G>T
  hgvsp: ENSP00000399862.2:p.Ala130Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.263G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3769G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3769G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.208G>T
  hgvsp: ENSP00000329376.6:p.Ala70Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.126G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.84G>T
  hgvsp: ENSP00000402979.1:p.Ala29Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.208G>T
  hgvsp: ENSP00000330060.5:p.Ala70Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.473G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-334G>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala130Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

3-32746394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746394
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746394
    reference: chr 3
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3768C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.389C>T
  hgvsp: ENSP00000399862.2:p.Ala130Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3768C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.264C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.209C>T
  hgvsp: ENSP00000329376.6:p.Ala70Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.209C>T
  hgvsp: ENSP00000330060.5:p.Ala70Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.127C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.85C>T
  hgvsp: ENSP00000402979.1:p.Ala29Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+940C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-333C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.474C>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala130Val
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

3-32746395-TGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746395
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746392
    reference: chr 3
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.129_131delGAG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-331_-329delGAG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3766_171-3764delGAG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.211_213delGAG
  hgvsp: ENSP00000329376.6:p.Glu71del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.211_213delGAG
  hgvsp: ENSP00000330060.5:p.Glu71del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.391_393delGAG
  hgvsp: ENSP00000399862.2:p.Glu131del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.266_268delGAG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3766_171-3764delGAG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.87_89delGAG
  hgvsp: ENSP00000402979.1:p.Glu30del
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+942_117+944delGAG
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.476_478delGAG
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu131del
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: TGAG
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

3-32746402-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746402
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746402
    reference: chr 3
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.272T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.397T>C
  hgvsp: ENSP00000399862.2:p.Phe133Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.93T>C
  hgvsp: ENSP00000402979.1:p.Phe32Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.217T>C
  hgvsp: ENSP00000330060.5:p.Phe73Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.135T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3760T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.482T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3760T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.217T>C
  hgvsp: ENSP00000329376.6:p.Phe73Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+948T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-325T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe133Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

3-32746407-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746407
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746407
    reference: chr 3
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.277A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.222A>G
  hgvsp: ENST00000331889.6:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.222A>G
  hgvsp: ENST00000328834.5:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+953A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.402A>G
  hgvsp: ENST00000454516.2:c.402A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3755A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-320A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.98A>G
  hgvsp: ENST00000416457.1:c.98A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.487A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3755A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.140A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys134Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

3-32746415-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746415
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746415
    reference: chr 3
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.230A>G
  hgvsp: ENSP00000330060.5:p.Gln77Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-312A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.495A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.148A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+961A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.410A>G
  hgvsp: ENSP00000399862.2:p.Gln137Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.285A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.106A>G
  hgvsp: ENSP00000402979.1:p.Gln36Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.230A>G
  hgvsp: ENSP00000329376.6:p.Gln77Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3747A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3747A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln137Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

3-32746423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746423
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746423
    reference: chr 3
allele count: 1
allele frequency: 8.284317786430287e-6
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.156A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.238A>G
  hgvsp: ENSP00000329376.6:p.Thr80Ala
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-304A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.238A>G
  hgvsp: ENSP00000330060.5:p.Thr80Ala
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3739A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.418A>G
  hgvsp: ENSP00000399862.2:p.Thr140Ala
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.503A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.114A>G
  hgvsp: ENSP00000402979.1:p.Thr39Ala
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.293A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+969A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3739A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr140Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-32746428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746428
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746428
    reference: chr 3
allele count: 5
allele frequency: 4.144012730407108e-5
allele num: 120656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.161T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3734T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.119T>C
  hgvsp: ENST00000416457.1:c.119T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-299T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.423T>C
  hgvsp: ENST00000454516.2:c.423T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.243T>C
  hgvsp: ENST00000331889.6:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3734T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+974T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.508T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.243T>C
  hgvsp: ENST00000328834.5:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.298T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Asp141Asp
num of homozygotes: 1
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-32746430-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746430
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746430
    reference: chr 3
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.245A>T
  hgvsp: ENSP00000330060.5:p.Asn82Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.163A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.510A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+976A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.245A>T
  hgvsp: ENSP00000329376.6:p.Asn82Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.425A>T
  hgvsp: ENSP00000399862.2:p.Asn142Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-297A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3732A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3732A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.121A>T
  hgvsp: ENSP00000402979.1:p.Asn41Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.300A>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn142Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

3-32746439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746439
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746439
    reference: chr 3
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.254A>G
  hgvsp: ENSP00000330060.5:p.Gln85Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3723A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-288A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.309A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.519A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.254A>G
  hgvsp: ENSP00000329376.6:p.Gln85Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.172A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.130A>G
  hgvsp: ENSP00000402979.1:p.Gln44Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.434A>G
  hgvsp: ENSP00000399862.2:p.Gln145Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+985A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3723A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln145Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

3-32746448-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746448
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746448
    reference: chr 3
allele count: 1
allele frequency: 8.337919188887221e-6
allele num: 119934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3714A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.139A>G
  hgvsp: ENSP00000402979.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.443A>G
  hgvsp: ENSP00000399862.2:p.Asn148Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-279A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+994A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.263A>G
  hgvsp: ENSP00000329376.6:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.318A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.263A>G
  hgvsp: ENSP00000330060.5:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.181A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3714A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.528A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn148Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

3-32746469-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746469
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746469
    reference: chr 3
allele count: 1
allele frequency: 8.551101381857983e-6
allele num: 116944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3693T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1015T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+5T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3693T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+5T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.459+5T>C
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

3-32746483-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746483
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746483
    reference: chr 3
allele count: 1
allele frequency: 8.809951721464566e-6
allele num: 113508
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3679T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1029T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3679T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+19T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+19T>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12857
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-32746487-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746487
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746487
    reference: chr 3
allele count: 1
allele frequency: 8.907098957869422e-6
allele num: 112270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3675T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3675T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+23T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1033T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6496
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-32746488-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746488
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746488
    reference: chr 3
allele count: 1
allele frequency: 8.909797213015431e-6
allele num: 112236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1034A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3674A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3674A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+24A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+24A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19062
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

3-32746489-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746489
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746490
    reference: chr 3
allele count: 1
allele frequency: 8.934474563550918e-6
allele num: 111926
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3667dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3667dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1041dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+31dupA
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+31dupA
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18822
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

3-32746498-TTGTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746498
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746493
    reference: chr 3
allele count: 1
allele frequency: 9.053378720938654e-6
allele num: 110456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+41_544+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+41_197+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+41_279+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+41_-263+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+41_155+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+41_279+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+41_334+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3657_171-3653delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3657_171-3653delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1051_117+1055delGTTCT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+41_459+45delGTTCT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 10030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: TTGTTC
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

3-32746503-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746503
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746503
    reference: chr 3
allele count: 1
allele frequency: 9.19709371838499e-6
allele num: 108730
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3659C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1049C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3659C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+39C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+39C>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8706
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

3-32746514-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32746514
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32746514
    reference: chr 3
allele count: 3
allele frequency: 2.826508884659594e-5
allele num: 106138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.279+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-3648T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.197+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.334+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.155+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.279+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-263+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.544+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.459+50T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.117+1060T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-3648T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7027
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9401
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4907
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

3-32750112-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750112
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750113
    reference: chr 3
allele count: 2
allele frequency: 1.66347833319471e-5
allele num: 120230
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-45dupT
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-45dupT
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

3-32750118-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750118
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750118
    reference: chr 3
allele count: 3
allele frequency: 2.493102416647276e-5
allele num: 120332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-44A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-44A>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13279
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

3-32750122-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750122
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750122
    reference: chr 3
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-40C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-40C>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-32750130-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750130
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750130
    reference: chr 3
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-32T>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-32T>A
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

3-32750141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750141
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750141
    reference: chr 3
allele count: 6
allele frequency: 4.96294335627316e-5
allele num: 120896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-21C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-21C>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

3-32750144-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750144
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750144
    reference: chr 3
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-18C>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-18C>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

3-32750147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750147
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750147
    reference: chr 3
allele count: 3
allele frequency: 2.478150968957029e-5
allele num: 121058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-15T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-15T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30265
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

3-32750158-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750158
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750158
    reference: chr 3
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.460-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.545-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.335-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.280-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.156-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-262-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.280-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.171-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.171-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.118-4A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.198-4A>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.460-4A>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-32750166-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750166
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750166
    reference: chr 3
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.175A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.339A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.122A>G
  hgvsp: ENSP00000402795.1:p.His41Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.549A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.160A>G
  hgvsp: ENSP00000402979.1:p.His54Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-258A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.202A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.464A>G
  hgvsp: ENSP00000399862.2:p.His155Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.175A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.284A>G
  hgvsp: ENSP00000329376.6:p.His95Arg
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.284A>G
  hgvsp: ENSP00000330060.5:p.His95Arg
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10750
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His155Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

3-32750167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750167
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750167
    reference: chr 3
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.285C>T
  hgvsp: ENST00000331889.6:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.285C>T
  hgvsp: ENST00000328834.5:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.176C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.161C>T
  hgvsp: ENST00000416457.1:c.161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.123C>T
  hgvsp: ENST00000435630.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-257C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.340C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.203C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.465C>T
  hgvsp: ENST00000454516.2:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.550C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.176C>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His155His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

3-32750170-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750170
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750170
    reference: chr 3
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.126A>T
  hgvsp: ENST00000435630.1:c.126A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.206A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.468A>T
  hgvsp: ENST00000454516.2:c.468A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.343A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-254A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.179A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.179A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.288A>T
  hgvsp: ENST00000331889.6:c.288A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.288A>T
  hgvsp: ENST00000328834.5:c.288A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.553A>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.164A>T
  hgvsp: ENST00000416457.1:c.164A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser156Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

3-32750188-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750188
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750188
    reference: chr 3
allele count: 11
allele frequency: 9.066033692677942e-5
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.361T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.197T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.306T>C
  hgvsp: ENST00000331889.6:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.306T>C
  hgvsp: ENST00000328834.5:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.197T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.182T>C
  hgvsp: ENST00000416457.1:c.182T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-236T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.144T>C
  hgvsp: ENST00000435630.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.224T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.571T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.486T>C
  hgvsp: ENST00000454516.2:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp162Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

3-32750211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750211
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750211
    reference: chr 3
allele count: 8
allele frequency: 6.59326168655634e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.329G>A
  hgvsp: ENSP00000329376.6:p.Ser110Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.220G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.384G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.509G>A
  hgvsp: ENSP00000399862.2:p.Ser170Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-213G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.23G>A
  hgvsp: ENSP00000392312.1:p.Ser8Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.205G>A
  hgvsp: ENSP00000402979.1:p.Ser69Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.220G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.167G>A
  hgvsp: ENSP00000402795.1:p.Ser56Asn
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.247G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.594G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.329G>A
  hgvsp: ENSP00000330060.5:p.Ser110Asn
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser170Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/3-32750213-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750213
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750213
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-211A>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.596A>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.169A>C
  hgvsp: ENSP00000402795.1:p.Met57Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.222A>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.25A>C
  hgvsp: ENSP00000392312.1:p.Met9Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.331A>C
  hgvsp: ENSP00000330060.5:p.Met111Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.331A>C
  hgvsp: ENSP00000329376.6:p.Met111Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.249A>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.207A>C
  hgvsp: ENSP00000402979.1:p.Met70Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.511A>C
  hgvsp: ENSP00000399862.2:p.Met171Leu
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.222A>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.386A>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met171Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

3-32750213-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750213
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750213
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.25A>G
  hgvsp: ENSP00000392312.1:p.Met9Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.386A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.331A>G
  hgvsp: ENSP00000329376.6:p.Met111Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-211A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.207A>G
  hgvsp: ENSP00000402979.1:p.Met70Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.169A>G
  hgvsp: ENSP00000402795.1:p.Met57Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.222A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.222A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.331A>G
  hgvsp: ENSP00000330060.5:p.Met111Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.511A>G
  hgvsp: ENSP00000399862.2:p.Met171Val
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.596A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.249A>G
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met171Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

3-32750223-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750223
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750223
    reference: chr 3
allele count: 3
allele frequency: 2.472676920033628e-5
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.259A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-201A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.179A>G
  hgvsp: ENSP00000402795.1:p.Tyr60Cys
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.232A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.521A>G
  hgvsp: ENSP00000399862.2:p.Tyr174Cys
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.232A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.35A>G
  hgvsp: ENSP00000392312.1:p.Tyr12Cys
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.606A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.341A>G
  hgvsp: ENSP00000329376.6:p.Tyr114Cys
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.217A>G
  hgvsp: ENSP00000402979.1:p.Tyr73Cys
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.396A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.341A>G
  hgvsp: ENSP00000330060.5:p.Tyr114Cys
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr174Cys
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

3-32750226-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750226
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750226
    reference: chr 3
allele count: 7
allele frequency: 5.769674590353104e-5
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.182A>G
  hgvsp: ENSP00000402795.1:p.Asn61Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.235A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.344A>G
  hgvsp: ENSP00000329376.6:p.Asn115Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.609A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.220A>G
  hgvsp: ENSP00000402979.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.235A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.524A>G
  hgvsp: ENSP00000399862.2:p.Asn175Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.344A>G
  hgvsp: ENSP00000330060.5:p.Asn115Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-198A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.399A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.262A>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.38A>G
  hgvsp: ENSP00000392312.1:p.Asn13Ser
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn175Ser
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

3-32750231-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750231
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750231
    reference: chr 3
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.187G>T
  hgvsp: ENSP00000402795.1:p.Ala63Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-193G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.614G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.240G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.529G>T
  hgvsp: ENSP00000399862.2:p.Ala177Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.240G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.267G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.225G>T
  hgvsp: ENSP00000402979.1:p.Ala76Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.349G>T
  hgvsp: ENSP00000330060.5:p.Ala117Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.349G>T
  hgvsp: ENSP00000329376.6:p.Ala117Ser
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.404G>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.43G>T
  hgvsp: ENSP00000392312.1:p.Ala15Ser
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala177Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

3-32750234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750234
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750234
    reference: chr 3
allele count: 3
allele frequency: 2.472880741204788e-5
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-190G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.407G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.532G>A
  hgvsp: ENSP00000399862.2:p.Val178Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.270G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.352G>A
  hgvsp: ENSP00000330060.5:p.Val118Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.228G>A
  hgvsp: ENSP00000402979.1:p.Val77Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.190G>A
  hgvsp: ENSP00000402795.1:p.Val64Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.243G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.352G>A
  hgvsp: ENSP00000329376.6:p.Val118Ile
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.617G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.243G>A
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.46G>A
  hgvsp: ENSP00000392312.1:p.Val16Ile
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val178Ile
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

3-32750235-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750235
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750235
    reference: chr 3
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.408T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.533T>G
  hgvsp: ENSP00000399862.2:p.Val178Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.353T>G
  hgvsp: ENSP00000329376.6:p.Val118Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.229T>G
  hgvsp: ENSP00000402979.1:p.Val77Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-189T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.244T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.191T>G
  hgvsp: ENSP00000402795.1:p.Val64Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.353T>G
  hgvsp: ENSP00000330060.5:p.Val118Gly
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.244T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.618T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.271T>G
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.47T>G
  hgvsp: ENSP00000392312.1:p.Val16Gly
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val178Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

3-32750238-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750238
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750238
    reference: chr 3
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.232T>C
  hgvsp: ENSP00000402979.1:p.Ile78Thr
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.621T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.194T>C
  hgvsp: ENSP00000402795.1:p.Ile65Thr
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.356T>C
  hgvsp: ENSP00000329376.6:p.Ile119Thr
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.536T>C
  hgvsp: ENSP00000399862.2:p.Ile179Thr
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.247T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.411T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.247T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-186T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.356T>C
  hgvsp: ENSP00000330060.5:p.Ile119Thr
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.50T>C
  hgvsp: ENSP00000392312.1:p.Ile17Thr
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.274T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile179Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

3-32750243-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750243
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750243
    reference: chr 3
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.541T>C
  hgvsp: ENSP00000399862.2:p.Tyr181His
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-181T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.361T>C
  hgvsp: ENSP00000329376.6:p.Tyr121His
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.279T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.237T>C
  hgvsp: ENSP00000402979.1:p.Tyr80His
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.199T>C
  hgvsp: ENSP00000402795.1:p.Tyr67His
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.416T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.252T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.55T>C
  hgvsp: ENSP00000392312.1:p.Tyr19His
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.626T>C
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.361T>C
  hgvsp: ENSP00000330060.5:p.Tyr121His
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.252T>C
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr181His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

3-32750252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32750252
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 32750252
    reference: chr 3
allele count: 16
allele frequency: 1.319304726409182e-4
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000463006
  gene symbol: CNOT10
  hgvsc: ENST00000463006.1:n.635C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000494439
  gene symbol: CNOT10
  hgvsc: ENST00000494439.1:n.261C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000329376
  ensembl transcript: ENST00000331889
  gene symbol: CNOT10
  hgvsc: ENST00000331889.6:c.370C>T
  hgvsp: ENSP00000329376.6:p.Arg124Trp
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000399862
  ensembl transcript: ENST00000454516
  gene symbol: CNOT10
  hgvsc: ENST00000454516.2:c.550C>T
  hgvsp: ENSP00000399862.2:p.Arg184Trp
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000556853
  gene symbol: CNOT10
  hgvsc: ENST00000556853.1:n.261C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402979
  ensembl transcript: ENST00000416457
  gene symbol: CNOT10
  hgvsc: ENST00000416457.1:c.246C>T
  hgvsp: ENSP00000402979.1:p.Arg83Trp
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000402795
  ensembl transcript: ENST00000435630
  gene symbol: CNOT10
  hgvsc: ENST00000435630.1:c.208C>T
  hgvsp: ENSP00000402795.1:p.Arg70Trp
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000392312
  ensembl transcript: ENST00000455381
  gene symbol: CNOT10
  hgvsc: ENST00000455381.1:c.64C>T
  hgvsp: ENSP00000392312.1:p.Arg22Trp
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000442552
  ensembl transcript: ENST00000538368
  gene symbol: CNOT10
  hgvsc: ENST00000538368.1:c.-172C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000485136
  gene symbol: CNOT10
  hgvsc: ENST00000485136.1:n.425C>T
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182973
  ensembl protein: ENSP00000330060
  ensembl transcript: ENST00000328834
  gene symbol: CNOT10
  hgvsc: ENST00000328834.5:c.370C>T
  hgvsp: ENSP00000330060.5:p.Arg124Trp
  variant of: http://identifiers.org/hgnc/23817
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000182973
  ensembl transcript: ENST00000466103
  gene symbol: CNOT10
  hgvsc: ENST00000466103.1:n.288C>T
  variant of: http://identifiers.org/hgnc/23817
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg184Trp
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 994
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2117
bin: 2.25e1
variant carriers: 8

GenotypeQuality
all individuals: 1129
bin: 4.25e1
variant carriers: 10

GenotypeQuality
all individuals: 17064
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1192
bin: 4.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1365
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1343
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 9605
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1225
bin: 2.75e1
variant carriers: 16

GenotypeQuality
all individuals: 679
bin: 7.5e0
variant carriers: 23

GenotypeQuality
all individuals: 5440
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1645
bin: 2.5e0
variant carriers: 13

GenotypeQuality
all individuals: 3424
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3558
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3159
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2443
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 4.423800044238001e-4
allele num: 9042
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.341790680653818e-3
allele num: 8198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 1.004566210045662e-3
allele num: 10950
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.320313487548982e-4
allele num: 15822
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 50
allele frequency: 8.140405717820976e-4
allele num: 61422
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

DP
type: SiteQuality
SIO_000300: 2.437961e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.157e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 3.965e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 8.8e-1

GenotypeQuality
all individuals: 1645
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17064
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 994
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5440
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9605
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628081143564195e-5
allele num: 61422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

DP
type: SiteQuality
SIO_000300: 2.437961e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

QD
type: SiteQuality
SIO_000300: 8.8e-1

FS
type: SiteQuality
SIO_000300: 3.965e0

VQSLOD
type: SiteQuality
SIO_000300: -7.157e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

GenotypeQuality
all individuals: 10283
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4068
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2827
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18320
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.562402349853134e-5
allele num: 64004
num of homozygotes: 0

Other
type: Population
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: 8436
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.14e-1

QD
type: SiteQuality
SIO_000300: 6.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

DP
type: SiteQuality
SIO_000300: 2.504767e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 3.327e0

GenotypeQuality
all individuals: 1676
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3782
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11668
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3503
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3747
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8059
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.980575754557227e-5
allele num: 40156
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.708e-1

FS
type: SiteQuality
SIO_000300: 7.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 2.865295e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

QD
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

GenotypeQuality
all individuals: 4122
bin: 7.5e0
variant carriers: 803

GenotypeQuality
all individuals: 2658
bin: 3.75e1
variant carriers: 567

GenotypeQuality
all individuals: 3747
bin: 2.25e1
variant carriers: 700

GenotypeQuality
all individuals: 1533
bin: 6.75e1
variant carriers: 314

GenotypeQuality
all individuals: 2036
bin: 4.75e1
variant carriers: 427

GenotypeQuality
all individuals: 1092
bin: 7.75e1
variant carriers: 271

GenotypeQuality
all individuals: 3168
bin: 2.75e1
variant carriers: 600

GenotypeQuality
all individuals: 959
bin: 8.25e1
variant carriers: 251

GenotypeQuality
all individuals: 3782
bin: 1.25e1
variant carriers: 769

GenotypeQuality
all individuals: 11668
bin: 2.5e0
variant carriers: 677

GenotypeQuality
all individuals: 1929
bin: 5.25e1
variant carriers: 437

GenotypeQuality
all individuals: 1676
bin: 5.75e1
variant carriers: 401

GenotypeQuality
all individuals: 2945
bin: 3.25e1
variant carriers: 601

GenotypeQuality
all individuals: 2304
bin: 4.25e1
variant carriers: 422

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 187

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 228

GenotypeQuality
all individuals: 8059
bin: 9.75e1
variant carriers: 4546

South Asian
type: Population
allele count: 2641
allele frequency: 2.358456867297732e-1
allele num: 11198
num of homozygotes: 1

East Asian
type: Population
allele count: 408
allele frequency: 7.950116913484022e-2
allele num: 5132
num of homozygotes: 0

Other
type: Population
allele count: 87
allele frequency: 1.469594594594595e-1
allele num: 592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 188
allele frequency: 4.161133244798584e-2
allele num: 4518
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 5214
allele frequency: 1.298436099213069e-1
allele num: 40156
num of homozygotes: 12

African
type: Population
allele count: 1052
allele frequency: 1.730263157894737e-1
allele num: 6080
num of homozygotes: 6

Latino
type: Population
allele count: 926
allele frequency: 1.357771260997067e-1
allele num: 6820
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.708e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 7.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

DP
type: SiteQuality
SIO_000300: 2.865295e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 8059
bin: 9.75e1
variant carriers: 351

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2304
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2036
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4122
bin: 7.5e0
variant carriers: 9

GenotypeQuality
all individuals: 3747
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 11668
bin: 2.5e0
variant carriers: 19

GenotypeQuality
all individuals: 2658
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3503
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1929
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3168
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1533
bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1676
bin: 5.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2756
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1092
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 959
bin: 8.25e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 290
allele frequency: 7.221834844107979e-3
allele num: 40156
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 2.346041055718475e-3
allele num: 6820
num of homozygotes: 1

East Asian
type: Population
allele count: 2
allele frequency: 3.897116134060795e-4
allele num: 5132
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 1.013513513513514e-2
allele num: 592
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 3.125e-3
allele num: 6080
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 57
allele frequency: 1.261620185922975e-2
allele num: 4518
num of homozygotes: 1

South Asian
type: Population
allele count: 51
allele frequency: 4.554384711555635e-3
allele num: 11198
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.865295e6

FS
type: SiteQuality
SIO_000300: 7.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

QD
type: SiteQuality
SIO_000300: 1.71e0

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.708e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 2756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11668
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 2945
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3503
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3747
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4122
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2036
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1676
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8059
bin: 9.75e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.426737494466578e-4
allele num: 4518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 2.490287877278613e-4
allele num: 40156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.708e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 7.37e-1

DP
type: SiteQuality
SIO_000300: 2.865295e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

GenotypeQuality
all individuals: 959
bin: 8.25e1
variant carriers: 315

GenotypeQuality
all individuals: 2036
bin: 4.75e1
variant carriers: 702

GenotypeQuality
all individuals: 1929
bin: 5.25e1
variant carriers: 627

GenotypeQuality
all individuals: 11668
bin: 2.5e0
variant carriers: 949

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 261

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 285

GenotypeQuality
all individuals: 1676
bin: 5.75e1
variant carriers: 549

GenotypeQuality
all individuals: 2658
bin: 3.75e1
variant carriers: 794

GenotypeQuality
all individuals: 3782
bin: 1.25e1
variant carriers: 1039

GenotypeQuality
all individuals: 4122
bin: 7.5e0
variant carriers: 1096

GenotypeQuality
all individuals: 3747
bin: 2.25e1
variant carriers: 994

GenotypeQuality
all individuals: 2756
bin: 6.25e1
variant carriers: 533

GenotypeQuality
all individuals: 1533
bin: 6.75e1
variant carriers: 436

GenotypeQuality
all individuals: 1092
bin: 7.75e1
variant carriers: 368

GenotypeQuality
all individuals: 8059
bin: 9.75e1
variant carriers: 2225

GenotypeQuality
all individuals: 3168
bin: 2.75e1
variant carriers: 898

GenotypeQuality
all individuals: 2945
bin: 3.25e1
variant carriers: 864

European (Non-Finnish)
type: Population
allele count: 6302
allele frequency: 1.569379420260982e-1
allele num: 40156
num of homozygotes: 0

East Asian
type: Population
allele count: 879
allele frequency: 1.712782540919719e-1
allele num: 5132
num of homozygotes: 0

African
type: Population
allele count: 758
allele frequency: 1.246710526315789e-1
allele num: 6080
num of homozygotes: 0

Latino
type: Population
allele count: 1038
allele frequency: 1.521994134897361e-1
allele num: 6820
num of homozygotes: 0

Other
type: Population
allele count: 93
allele frequency: 1.570945945945946e-1
allele num: 592
num of homozygotes: 0

South Asian
type: Population
allele count: 1526
allele frequency: 1.362743347026255e-1
allele num: 11198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 414
allele frequency: 9.163346613545817e-2
allele num: 4518
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.708e-1

QD
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 2.865295e6

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

GenotypeQuality
all individuals: 11668
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 3747
bin: 2.25e1
variant carriers: 11

GenotypeQuality
all individuals: 3503
bin: 1.75e1
variant carriers: 14

GenotypeQuality
all individuals: 3782
bin: 1.25e1
variant carriers: 13

GenotypeQuality
all individuals: 3168
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2036
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2945
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2756
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2304
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 8059
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1533
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 823
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2658
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1676
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1929
bin: 5.25e1
variant carriers: 2

Other
type: Population
allele count: 1
allele frequency: 1.689189189189189e-3
allele num: 592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 6.640106241699867e-4
allele num: 4518
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 7.331378299120235e-4
allele num: 6820
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.578947368421052e-4
allele num: 6080
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.948558067030398e-4
allele num: 5132
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.358099660653688e-4
allele num: 11198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 1.09572666600259e-3
allele num: 40156
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.37e-1

DP
type: SiteQuality
SIO_000300: 2.865295e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.92e-1

QD
type: SiteQuality
SIO_000300: 1.71e0

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.708e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 1124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21355
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11671
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1495
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.804891731179177e-5
allele num: 35652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.950000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 1.1215e1

DP
type: SiteQuality
SIO_000300: 2.929276e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.126e0

QD
type: SiteQuality
SIO_000300: 5.2e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: -3.409e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.449e0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1395
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3375
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5629
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31793
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2906
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

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

Latino
type: Population
allele count: 52
allele frequency: 4.520166898470098e-3
allele num: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 1.979559e6

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.567e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5580
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 453
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1392
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516714190377965e-5
allele num: 65932
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.026061974143238e-4
allele num: 9746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.304e0

DP
type: SiteQuality
SIO_000300: 1.977206e6

VQSLOD
type: SiteQuality
SIO_000300: 5.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

QD
type: SiteQuality
SIO_000300: 1.078e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQ
type: SiteQuality
SIO_000300: 5.926e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3247
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 8.75e1
variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66174
num of homozygotes: 0

African
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allele count: 47
allele frequency: 4.745557350565428e-3
allele num: 9904
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
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SIO_000300: 2.33e1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

BaseQRankSum
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SIO_000300: 2.8e0

FS
type: SiteQuality
SIO_000300: 5.27e-1

DP
type: SiteQuality
SIO_000300: 1.946791e6

VQSLOD
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SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.009489198465576e-4
allele num: 9906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66174
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.4273e1

ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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SIO_000300: -1.849e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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SIO_000300: -7.49e-1

VQSLOD
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510345869204048e-5
allele num: 66210
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -2.06e0

QD
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.508e0

MQ
type: SiteQuality
SIO_000300: 6.067e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.17e-1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

DP
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SIO_000300: 1.946833e6

InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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FS
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MQ
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SIO_000300: 5.963e1

MQRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.554e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.821714840903571e-4
allele num: 16468
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 1.002405773857257e-4
allele num: 9976
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509251713000694e-5
allele num: 66258
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: -1.894e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509206157561123e-5
allele num: 66260
num of homozygotes: 0

Other
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Latino
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MQ
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
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European (Finnish)
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Other
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European (Non-Finnish)
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allele frequency: 6.036278030966107e-5
allele num: 66266
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66312
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Latino
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East Asian
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South Asian
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Other
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 66442
num of homozygotes: 0

Latino
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Other
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East Asian
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European (Finnish)
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South Asian
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QD
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ClippingRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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SIO_000300: 1.16e0

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 10056
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66394
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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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Other
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South Asian
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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African
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Latino
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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South Asian
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East Asian
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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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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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
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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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num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66434
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South Asian
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QD
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FS
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -8.0e-4

MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66486
num of homozygotes: 0

African
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South Asian
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Other
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DP
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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SIO_000300: 3.33e-1

InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66490
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African
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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SIO_000300: 1.666e0

ReadPosRankSum
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DP
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SIO_000300: 1.951904e6

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

East Asian
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allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 904
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele num: 10064
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East Asian
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South Asian
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66466
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Latino
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South Asian
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European (Non-Finnish)
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.184e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

FS
type: SiteQuality
SIO_000300: 6.830000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

DP
type: SiteQuality
SIO_000300: 1.947659e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.576e0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4816
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.942382e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.572e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.244e1

GenotypeQuality
all individuals: 2212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4811
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1241
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.253908692933083e-5
allele num: 15990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66222
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.67e-1

FS
type: SiteQuality
SIO_000300: 1.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

DP
type: SiteQuality
SIO_000300: 1.92991e6

QD
type: SiteQuality
SIO_000300: 1.029e1

GenotypeDepth
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2595
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variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14308
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65202
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.897e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.454e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.865906e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.64e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.165e-1

QD
type: SiteQuality
SIO_000300: 1.515e1

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6591
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2455
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
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variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4800
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7160
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63656
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.771783e6

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

FS
type: SiteQuality
SIO_000300: 1.362e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 2.452e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.0e-2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.062473438164046e-4
allele num: 9412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.289e0

VQSLOD
type: SiteQuality
SIO_000300: -6.383e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.724902e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.85e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 953
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.062699256110521e-4
allele num: 9410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63188
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 3.736e0

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.72365e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.25e1
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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bin: 9.75e1
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GenotypeQuality
all individuals: 2358
bin: 7.25e1
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GenotypeQuality
all individuals: 297
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.183151916706105e-4
allele num: 8452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e0

FS
type: SiteQuality
SIO_000300: 2.632e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

DP
type: SiteQuality
SIO_000300: 1.714417e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

QD
type: SiteQuality
SIO_000300: 1.659e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.60040970488445e-5
allele num: 62484
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.622e1

DP
type: SiteQuality
SIO_000300: 1.637711e6

BaseQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 3.68e0

MQRankSum
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SIO_000300: -2.023e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-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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bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10814
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.621428803061258e-5
allele num: 61674
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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InbreedingCoeff
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SIO_000300: 1.2e-3

BaseQRankSum
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SIO_000300: -1.961e0

MQRankSum
type: SiteQuality
SIO_000300: -1.226e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.588106e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.962122465182441e-5
allele num: 60458
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.582e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

BaseQRankSum
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SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.529438e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.665e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66298
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.743679163034002e-4
allele num: 11470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 896
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

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

BaseQRankSum
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SIO_000300: -7.11e-1

ReadPosRankSum
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MQRankSum
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QD
type: SiteQuality
SIO_000300: 1.451e1

ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.970562e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.522840343735866e-5
allele num: 66330
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.902e0

DP
type: SiteQuality
SIO_000300: 1.982687e6

QD
type: SiteQuality
SIO_000300: 8.5e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -4.68e-1

MQ
type: SiteQuality
SIO_000300: 5.723e1

FS
type: SiteQuality
SIO_000300: 2.0887e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506296318611797e-5
allele num: 66388
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16454
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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QD
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DP
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.936416184971098e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.34e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.01662e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.507e0

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

GenotypeQuality
all individuals: 8809
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3881
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8652
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2716
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0376e1

VQSLOD
type: SiteQuality
SIO_000300: -2.327e0

DP
type: SiteQuality
SIO_000300: 2.017974e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.81e-1

QD
type: SiteQuality
SIO_000300: 1.034e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: -1.585e0

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

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3885
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2718
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8653
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502476361999099e-5
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

DP
type: SiteQuality
SIO_000300: 2.019322e6

FS
type: SiteQuality
SIO_000300: 2.573e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.57e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

GenotypeDepth
all individuals: 229
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8653
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8839
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1631
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3894
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 2.021745e6

QD
type: SiteQuality
SIO_000300: 1.226e1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.014e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30477
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2717
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8838
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3895
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8654
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.759e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.825e0

FS
type: SiteQuality
SIO_000300: 4.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

DP
type: SiteQuality
SIO_000300: 2.022535e6

QD
type: SiteQuality
SIO_000300: 6.86e0

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

GenotypeQuality
all individuals: 2717
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

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

GenotypeQuality
all individuals: 3894
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8655
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 30477
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998770504093322e-5
allele num: 66694
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
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: 10368
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.015e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

DP
type: SiteQuality
SIO_000300: 2.022737e6

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

FS
type: SiteQuality
SIO_000300: 7.783e0

QD
type: SiteQuality
SIO_000300: 1.131e1

GenotypeQuality
all individuals: 30486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
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: 906
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

FS
type: SiteQuality
SIO_000300: 1.4334e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.464e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.384e-1

DP
type: SiteQuality
SIO_000300: 2.022922e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 8662
bin: 9.75e1
variant carriers: 11

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

African
type: Population
allele count: 8
allele frequency: 7.695267410542517e-4
allele num: 10396
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 1.127e0

DP
type: SiteQuality
SIO_000300: 2.024221e6

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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Other
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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MQRankSum
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DP
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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VQSLOD
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MQ
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BaseQRankSum
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QD
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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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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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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FS
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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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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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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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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South Asian
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East Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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SIO_000300: -3.007e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.83e-2

DP
type: SiteQuality
SIO_000300: 2.022978e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.172e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.382e0

FS
type: SiteQuality
SIO_000300: 1.034e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeDepth
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2219
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8843
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8645
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 11546
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 7.08e-1

FS
type: SiteQuality
SIO_000300: 1.064e0

DP
type: SiteQuality
SIO_000300: 2.022765e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.21e-1

QD
type: SiteQuality
SIO_000300: 1.229e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeDepth
all individuals: 204
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30351
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1629
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3875
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8644
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1219
bin: 8.75e1
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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.53e-2

FS
type: SiteQuality
SIO_000300: 6.638e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

DP
type: SiteQuality
SIO_000300: 2.022722e6

VQSLOD
type: SiteQuality
SIO_000300: -4.286e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 1.176e1

GenotypeDepth
all individuals: 1378
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3874
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8842
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8643
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 30329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 2.022648e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.73e-1

QD
type: SiteQuality
SIO_000300: 1.492e1

VQSLOD
type: SiteQuality
SIO_000300: 4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.01e-1

FS
type: SiteQuality
SIO_000300: 3.626e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 1383
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 229
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 377
bin: 7.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30190
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0