http://identifiers.org/exac.variant/5-154251266-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251266
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251266
    reference: chr 5
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-24C>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-24C>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

5-154251267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251267
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251267
    reference: chr 5
allele count: 187
allele frequency: 1.543158937118336e-3
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-23C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-23C>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 30381
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

5-154251270-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251270
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251270
    reference: chr 5
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-20T>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7969
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

5-154251277-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251277
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251277
    reference: chr 5
allele count: 4
allele frequency: 3.298860243785772e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-13T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-13T>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

5-154251278-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251278
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251278
    reference: chr 5
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-12A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-12A>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

5-154251278-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251278
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251278
    reference: chr 5
allele count: 4
allele frequency: 3.298588204248581e-5
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-12A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-12A>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

5-154251283-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251283
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251283
    reference: chr 5
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.156-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.474-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.156-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.474-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.380-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-19-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.312-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*121-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.312-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.156-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.474-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.312-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.156-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*221-7C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.156-7C>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 30604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.474-7C>G
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

5-154251294-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251294
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251294
    reference: chr 5
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-15T>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.160T>G
  hgvsp: ENSP00000428359.1:p.Tyr54Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.478T>G
  hgvsp: ENSP00000384747.2:p.Tyr160Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.316T>G
  hgvsp: ENSP00000428550.1:p.Tyr106Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.316T>G
  hgvsp: ENSP00000430833.1:p.Tyr106Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.160T>G
  hgvsp: ENSP00000428305.1:p.Tyr54Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.478T>G
  hgvsp: ENSP00000285896.6:p.Tyr160Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.478T>G
  hgvsp: ENSP00000430493.1:p.Tyr160Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.384T>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.160T>G
  hgvsp: ENSP00000428565.1:p.Tyr54Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.160T>G
  hgvsp: ENSP00000429882.1:p.Tyr54Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.316T>G
  hgvsp: ENSP00000429394.1:p.Tyr106Asp
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*125T>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*225T>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.160T>G
  hgvsp: ENSP00000431034.1:p.Tyr54Asp
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr160Asp
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

5-154251295-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251295
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251295
    reference: chr 5
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.161A>G
  hgvsp: ENSP00000431034.1:p.Tyr54Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.317A>G
  hgvsp: ENSP00000430833.1:p.Tyr106Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.479A>G
  hgvsp: ENSP00000285896.6:p.Tyr160Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.161A>G
  hgvsp: ENSP00000428305.1:p.Tyr54Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.317A>G
  hgvsp: ENSP00000429394.1:p.Tyr106Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.161A>G
  hgvsp: ENSP00000429882.1:p.Tyr54Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.479A>G
  hgvsp: ENSP00000430493.1:p.Tyr160Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.161A>G
  hgvsp: ENSP00000428359.1:p.Tyr54Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-14A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.479A>G
  hgvsp: ENSP00000384747.2:p.Tyr160Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.161A>G
  hgvsp: ENSP00000428565.1:p.Tyr54Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*226A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.385A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.317A>G
  hgvsp: ENSP00000428550.1:p.Tyr106Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*126A>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr160Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

5-154251303-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251303
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251303
    reference: chr 5
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*234G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.169G>T
  hgvsp: ENSP00000429882.1:p.Gly57Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.169G>T
  hgvsp: ENSP00000428305.1:p.Gly57Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.325G>T
  hgvsp: ENSP00000430833.1:p.Gly109Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*134G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.487G>T
  hgvsp: ENSP00000285896.6:p.Gly163Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.169G>T
  hgvsp: ENSP00000428359.1:p.Gly57Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.393G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.325G>T
  hgvsp: ENSP00000429394.1:p.Gly109Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.487G>T
  hgvsp: ENSP00000384747.2:p.Gly163Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.169G>T
  hgvsp: ENSP00000431034.1:p.Gly57Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.487G>T
  hgvsp: ENSP00000430493.1:p.Gly163Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-6G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.325G>T
  hgvsp: ENSP00000428550.1:p.Gly109Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.169G>T
  hgvsp: ENSP00000428565.1:p.Gly57Cys
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly163Cys
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

5-154251308-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251308
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251308
    reference: chr 5
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.174T>C
  hgvsp: ENST00000520671.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.492T>C
  hgvsp: ENST00000403027.2:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.330T>C
  hgvsp: ENST00000519404.1:c.330T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.174T>C
  hgvsp: ENST00000519903.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.330T>C
  hgvsp: ENST00000518775.1:c.330T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.492T>C
  hgvsp: ENST00000517876.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.330T>C
  hgvsp: ENST00000522458.1:c.330T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.492T>C
  hgvsp: ENST00000285896.6:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.174T>C
  hgvsp: ENST00000521583.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*239T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.398T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.174T>C
  hgvsp: ENST00000523698.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.-1T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.174T>C
  hgvsp: ENST00000521450.1:c.174T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*139T>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr164Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum

5-154251331-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251331
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251331
    reference: chr 5
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.197C>G
  hgvsp: ENSP00000428305.1:p.Ser66Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.197C>G
  hgvsp: ENSP00000431034.1:p.Ser66Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.353C>G
  hgvsp: ENSP00000429394.1:p.Ser118Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.421C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.353C>G
  hgvsp: ENSP00000430833.1:p.Ser118Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.515C>G
  hgvsp: ENSP00000285896.6:p.Ser172Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.353C>G
  hgvsp: ENSP00000428550.1:p.Ser118Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.23C>G
  hgvsp: ENSP00000429576.1:p.Ser8Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.197C>G
  hgvsp: ENSP00000428565.1:p.Ser66Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.197C>G
  hgvsp: ENSP00000429882.1:p.Ser66Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*262C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*162C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.197C>G
  hgvsp: ENSP00000428359.1:p.Ser66Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.515C>G
  hgvsp: ENSP00000430493.1:p.Ser172Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.515C>G
  hgvsp: ENSP00000384747.2:p.Ser172Cys
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30689
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser172Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

5-154251333-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251333
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251333
    reference: chr 5
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.517C>T
  hgvsp: ENSP00000430493.1:p.Arg173Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.25C>T
  hgvsp: ENSP00000429576.1:p.Arg9Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.517C>T
  hgvsp: ENSP00000384747.2:p.Arg173Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.355C>T
  hgvsp: ENSP00000429394.1:p.Arg119Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*164C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*264C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.517C>T
  hgvsp: ENSP00000285896.6:p.Arg173Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.199C>T
  hgvsp: ENSP00000429882.1:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.355C>T
  hgvsp: ENSP00000430833.1:p.Arg119Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.199C>T
  hgvsp: ENSP00000428565.1:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.199C>T
  hgvsp: ENSP00000428359.1:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.199C>T
  hgvsp: ENSP00000431034.1:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.355C>T
  hgvsp: ENSP00000428550.1:p.Arg119Cys
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.423C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.199C>T
  hgvsp: ENSP00000428305.1:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16726
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg173Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP

5-154251334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251334
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251334
    reference: chr 5
allele count: 6
allele frequency: 4.944131316127757e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.356G>A
  hgvsp: ENSP00000429394.1:p.Arg119His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.424G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.518G>A
  hgvsp: ENSP00000384747.2:p.Arg173His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.200G>A
  hgvsp: ENSP00000429882.1:p.Arg67His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.518G>A
  hgvsp: ENSP00000430493.1:p.Arg173His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.356G>A
  hgvsp: ENSP00000430833.1:p.Arg119His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.356G>A
  hgvsp: ENSP00000428550.1:p.Arg119His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*165G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.26G>A
  hgvsp: ENSP00000429576.1:p.Arg9His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*265G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.518G>A
  hgvsp: ENSP00000285896.6:p.Arg173His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.200G>A
  hgvsp: ENSP00000428359.1:p.Arg67His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.200G>A
  hgvsp: ENSP00000428305.1:p.Arg67His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.200G>A
  hgvsp: ENSP00000428565.1:p.Arg67His
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.200G>A
  hgvsp: ENSP00000431034.1:p.Arg67His
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg173His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

5-154251340-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251340
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251340
    reference: chr 5
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.206C>G
  hgvsp: ENSP00000431034.1:p.Pro69Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.206C>G
  hgvsp: ENSP00000428305.1:p.Pro69Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.524C>G
  hgvsp: ENSP00000384747.2:p.Pro175Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.206C>G
  hgvsp: ENSP00000429882.1:p.Pro69Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.206C>G
  hgvsp: ENSP00000428565.1:p.Pro69Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.362C>G
  hgvsp: ENSP00000428550.1:p.Pro121Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.32C>G
  hgvsp: ENSP00000429576.1:p.Pro11Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.362C>G
  hgvsp: ENSP00000430833.1:p.Pro121Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.524C>G
  hgvsp: ENSP00000285896.6:p.Pro175Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*171C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.362C>G
  hgvsp: ENSP00000429394.1:p.Pro121Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.206C>G
  hgvsp: ENSP00000428359.1:p.Pro69Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.430C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*271C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.524C>G
  hgvsp: ENSP00000430493.1:p.Pro175Arg
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro175Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

5-154251341-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251341
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251341
    reference: chr 5
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*272A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.207A>G
  hgvsp: ENST00000521450.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.33A>G
  hgvsp: ENST00000524105.1:c.33A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.363A>G
  hgvsp: ENST00000518775.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.207A>G
  hgvsp: ENST00000520671.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.525A>G
  hgvsp: ENST00000285896.6:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428550
  ensembl transcript: ENST00000522458
  gene symbol: CNOT8
  hgvsc: ENST00000522458.1:c.363A>G
  hgvsp: ENST00000522458.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*172A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.363A>G
  hgvsp: ENST00000519404.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.207A>G
  hgvsp: ENST00000523698.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.431A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.207A>G
  hgvsp: ENST00000519903.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.525A>G
  hgvsp: ENST00000517876.1:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.207A>G
  hgvsp: ENST00000521583.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.525A>G
  hgvsp: ENST00000403027.2:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro175Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

5-154251364-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251364
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251364
    reference: chr 5
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.548A>G
  hgvsp: ENSP00000285896.6:p.His183Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.454A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.230A>G
  hgvsp: ENSP00000428359.1:p.His77Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.230A>G
  hgvsp: ENSP00000429882.1:p.His77Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.56A>G
  hgvsp: ENSP00000429576.1:p.His19Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*195A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*295A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.386A>G
  hgvsp: ENSP00000429394.1:p.His129Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.548A>G
  hgvsp: ENSP00000384747.2:p.His183Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.386A>G
  hgvsp: ENSP00000430833.1:p.His129Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.230A>G
  hgvsp: ENSP00000428565.1:p.His77Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.230A>G
  hgvsp: ENSP00000431034.1:p.His77Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.548A>G
  hgvsp: ENSP00000430493.1:p.His183Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.230A>G
  hgvsp: ENSP00000428305.1:p.His77Arg
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His183Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS

5-154251365-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251365
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251365
    reference: chr 5
allele count: 8
allele frequency: 6.603602265035577e-5
allele num: 121146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.231T>C
  hgvsp: ENST00000521450.1:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*296T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.549T>C
  hgvsp: ENST00000285896.6:c.549T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.549T>C
  hgvsp: ENST00000403027.2:c.549T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*196T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.387T>C
  hgvsp: ENST00000518775.1:c.387T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.549T>C
  hgvsp: ENST00000517876.1:c.549T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.387T>C
  hgvsp: ENST00000519404.1:c.387T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.231T>C
  hgvsp: ENST00000521583.1:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.455T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.231T>C
  hgvsp: ENST00000520671.1:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.57T>C
  hgvsp: ENST00000524105.1:c.57T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.231T>C
  hgvsp: ENST00000523698.1:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.231T>C
  hgvsp: ENST00000519903.1:c.231T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His183His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

5-154251374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251374
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251374
    reference: chr 5
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.464C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.558C>T
  hgvsp: ENST00000403027.2:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.66C>T
  hgvsp: ENST00000524105.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.240C>T
  hgvsp: ENST00000520671.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.240C>T
  hgvsp: ENST00000523698.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.240C>T
  hgvsp: ENST00000521583.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.240C>T
  hgvsp: ENST00000519903.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*205C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*305C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.396C>T
  hgvsp: ENST00000518775.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.396C>T
  hgvsp: ENST00000519404.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.558C>T
  hgvsp: ENST00000285896.6:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.558C>T
  hgvsp: ENST00000517876.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.240C>T
  hgvsp: ENST00000521450.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn186Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

5-154251381-T-TGAGTAGTTTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251381
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251391
    reference: chr 5
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: TGAGTAGTTTA
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsp: ENSP00000430493.1:p.Phe189Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsp: ENSP00000428565.1:p.Phe83Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsp: ENSP00000384747.2:p.Phe189Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsp: ENSP00000285896.6:p.Phe189Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsp: ENSP00000430833.1:p.Phe135Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsp: ENSP00000428305.1:p.Phe83Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.73_74insGAGTAGTTTA
  hgvsp: ENSP00000429576.1:p.Phe25Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsp: ENSP00000431034.1:p.Phe83Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsp: ENSP00000429394.1:p.Phe135Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsp: ENSP00000428359.1:p.Phe83Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsp: ENSP00000429882.1:p.Phe83Ter
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe189Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

5-154251383-C-CGTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251383
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251386
    reference: chr 5
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: CGTA
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.567_568insGTA
  hgvsp: ENSP00000285896.6:p.Phe189_Pro190insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*314_*315insGTA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*214_*215insGTA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.567_568insGTA
  hgvsp: ENSP00000384747.2:p.Phe189_Pro190insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.405_406insGTA
  hgvsp: ENSP00000429394.1:p.Phe135_Pro136insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.249_250insGTA
  hgvsp: ENSP00000428565.1:p.Phe83_Pro84insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.249_250insGTA
  hgvsp: ENSP00000428305.1:p.Phe83_Pro84insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.249_250insGTA
  hgvsp: ENSP00000429882.1:p.Phe83_Pro84insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.249_250insGTA
  hgvsp: ENSP00000431034.1:p.Phe83_Pro84insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.405_406insGTA
  hgvsp: ENSP00000430833.1:p.Phe135_Pro136insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.75_76insGTA
  hgvsp: ENSP00000429576.1:p.Phe25_Pro26insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.249_250insGTA
  hgvsp: ENSP00000428359.1:p.Phe83_Pro84insVal
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.473_474insGTA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.567_568insGTA
  hgvsp: ENSP00000430493.1:p.Phe189_Pro190insVal
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe189_Pro190insVal
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

5-154251390-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251390
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251390
    reference: chr 5
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.574A>G
  hgvsp: ENSP00000384747.2:p.Ile192Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*321A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428359
  ensembl transcript: ENST00000519903
  gene symbol: CNOT8
  hgvsc: ENST00000519903.1:c.256A>G
  hgvsp: ENST00000519903.1:c.256A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.82A>G
  hgvsp: ENSP00000429576.1:p.Ile28Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.256A>G
  hgvsp: ENSP00000428305.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.256A>G
  hgvsp: ENSP00000428565.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.412A>G
  hgvsp: ENSP00000430833.1:p.Ile138Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.256A>G
  hgvsp: ENSP00000429882.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.574A>G
  hgvsp: ENSP00000430493.1:p.Ile192Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.480A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.574A>G
  hgvsp: ENSP00000285896.6:p.Ile192Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*221A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.412A>G
  hgvsp: ENSP00000429394.1:p.Ile138Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.256A>G
  hgvsp: ENSP00000431034.1:p.Ile86Val
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile192Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

5-154251410-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251410
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251410
    reference: chr 5
allele count: 2
allele frequency: 1.690274162469152e-5
allele num: 118324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*341G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.276G>C
  hgvsp: ENST00000523698.1:c.276G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.500G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.276G>C
  hgvsp: ENST00000521583.1:c.276G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.432G>C
  hgvsp: ENST00000518775.1:c.432G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.102G>C
  hgvsp: ENST00000524105.1:c.102G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.594G>C
  hgvsp: ENST00000517876.1:c.594G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*241G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.276G>C
  hgvsp: ENST00000520671.1:c.276G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.594G>C
  hgvsp: ENST00000403027.2:c.594G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.276G>C
  hgvsp: ENST00000521450.1:c.276G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.432G>C
  hgvsp: ENST00000519404.1:c.432G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.594G>C
  hgvsp: ENST00000285896.6:c.594G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu198Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

5-154251420-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251420
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251420
    reference: chr 5
allele count: 1
allele frequency: 8.636622735045688e-6
allele num: 115786
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.604T>A
  hgvsp: ENSP00000430493.1:p.Cys202Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*351T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.442T>A
  hgvsp: ENSP00000429394.1:p.Cys148Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.112T>A
  hgvsp: ENSP00000429576.1:p.Cys38Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.286T>A
  hgvsp: ENSP00000428565.1:p.Cys96Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.510T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*251T>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.286T>A
  hgvsp: ENSP00000431034.1:p.Cys96Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.604T>A
  hgvsp: ENSP00000285896.6:p.Cys202Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.604T>A
  hgvsp: ENSP00000384747.2:p.Cys202Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.286T>A
  hgvsp: ENSP00000429882.1:p.Cys96Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.286T>A
  hgvsp: ENSP00000428305.1:p.Cys96Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.442T>A
  hgvsp: ENSP00000430833.1:p.Cys148Ser
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15121
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys202Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

5-154251452-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251452
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251451
    reference: chr 5
allele count: 1
allele frequency: 9.607624610891203e-6
allele num: 104084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+20delA
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+20delA
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17678
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: TA
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-154251459-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251459
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251459
    reference: chr 5
allele count: 17
allele frequency: 1.667582201993251e-4
allele num: 101944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+25A>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6884
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20126
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

5-154251460-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251460
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251460
    reference: chr 5
allele count: 1
allele frequency: 9.821639035122181e-6
allele num: 101816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+26G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+26G>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

5-154251467-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251467
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251464
    reference: chr 5
allele count: 6
allele frequency: 6.034881615738971e-5
allele num: 99422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+37_300+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+37_*265+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+37_456+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+37_618+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+37_618+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+37_618+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+37_300+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+37_300+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+37_300+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+37_456+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+37_126+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+37_*365+39delAAG
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+37_524+39delAAG
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20374
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: AAAG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

5-154251471-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251471
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251471
    reference: chr 5
allele count: 3
allele frequency: 3.091253812546369e-5
allele num: 97048
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+37A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+37A>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

5-154251473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251473
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251473
    reference: chr 5
allele count: 31
allele frequency: 3.209508427547935e-4
allele num: 96588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+39G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+39G>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19585
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-154251473-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251473
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251473
    reference: chr 5
allele count: 3
allele frequency: 3.105975897627034e-5
allele num: 96588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+39G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+39G>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

5-154251477-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251477
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251477
    reference: chr 5
allele count: 1
allele frequency: 1.050729206069012e-5
allele num: 95172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+43A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+43A>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-154251480-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154251480
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154251480
    reference: chr 5
allele count: 1
allele frequency: 1.077934677158564e-5
allele num: 92770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.126+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.456+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.300+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*365+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.618+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.618+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*265+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.300+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.618+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.524+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.456+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.300+46A>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.300+46A>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

5-154252074-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252074
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252074
    reference: chr 5
allele count: 1
allele frequency: 1.117218572641552e-5
allele num: 89508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.127-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.619-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.301-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.301-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.619-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.301-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.525-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.301-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.457-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*266-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*366-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.457-27T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.619-27T>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

5-154252076-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252076
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252076
    reference: chr 5
allele count: 1
allele frequency: 1.099505222649808e-5
allele num: 90950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.301-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.619-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*366-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.301-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*266-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.301-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.127-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.457-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.457-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.619-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.301-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.525-25A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.619-25A>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-154252078-CTTTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252078
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252074
    reference: chr 5
allele count: 6
allele frequency: 6.507168730885192e-5
allele num: 92206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.525-20_525-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.301-20_301-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.619-20_619-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.457-20_457-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*366-20_*366-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.619-20_619-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.457-20_457-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*266-20_*266-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.301-20_301-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.127-20_127-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.301-20_301-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.619-20_619-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.301-20_301-17delTGTT
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11271
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24540
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: CTTTG
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

5-154252082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252082
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252082
    reference: chr 5
allele count: 1
allele frequency: 1.040496108544554e-5
allele num: 96108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.301-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.525-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*266-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.301-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.301-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.127-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.457-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*366-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.619-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.457-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.619-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.619-19G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.301-19G>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

5-154252092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252092
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252092
    reference: chr 5
allele count: 1
allele frequency: 9.247614115558185e-6
allele num: 108136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.525-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.619-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.619-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.457-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.301-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*366-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.127-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.457-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.301-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.301-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*266-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.619-9C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.301-9C>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP

5-154252098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252098
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252098
    reference: chr 5
allele count: 1
allele frequency: 8.844548220476899e-6
allele num: 113064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.301-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*366-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.619-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*266-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.127-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.301-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.301-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.457-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.619-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.457-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.525-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.301-3C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.619-3C>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.619-3C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

5-154252121-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252121
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252121
    reference: chr 5
allele count: 11
allele frequency: 9.214119381481295e-5
allele num: 119382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.321T>C
  hgvsp: ENST00000521583.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*286T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.639T>C
  hgvsp: ENST00000403027.2:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.639T>C
  hgvsp: ENST00000517876.1:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.321T>C
  hgvsp: ENST00000520671.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.477T>C
  hgvsp: ENST00000518775.1:c.477T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*386T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.321T>C
  hgvsp: ENST00000523698.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.639T>C
  hgvsp: ENST00000285896.6:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.545T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.321T>C
  hgvsp: ENST00000521450.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.147T>C
  hgvsp: ENST00000524105.1:c.147T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.477T>C
  hgvsp: ENST00000519404.1:c.477T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala213Ala
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

5-154252123-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252123
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252123
    reference: chr 5
allele count: 2
allele frequency: 1.673276107290464e-5
allele num: 119526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.479A>T
  hgvsp: ENSP00000430833.1:p.Asp160Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.323A>T
  hgvsp: ENSP00000428565.1:p.Asp108Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.641A>T
  hgvsp: ENSP00000384747.2:p.Asp214Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.479A>T
  hgvsp: ENSP00000429394.1:p.Asp160Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.323A>T
  hgvsp: ENSP00000429882.1:p.Asp108Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.149A>T
  hgvsp: ENSP00000429576.1:p.Asp50Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*288A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.323A>T
  hgvsp: ENSP00000428305.1:p.Asp108Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000155508
  ensembl transcript: ENST00000522139
  gene symbol: CNOT8
  hgvsc: ENST00000522139.1:n.547A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.641A>T
  hgvsp: ENSP00000430493.1:p.Asp214Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*388A>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.323A>T
  hgvsp: ENSP00000431034.1:p.Asp108Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.641A>T
  hgvsp: ENSP00000285896.6:p.Asp214Val
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp214Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

5-154252144-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252144
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252144
    reference: chr 5
allele count: 4
allele frequency: 3.323528923010452e-5
allele num: 120354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.344T>C
  hgvsp: ENSP00000428565.1:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.344T>C
  hgvsp: ENSP00000431034.1:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.662T>C
  hgvsp: ENSP00000285896.6:p.Ile221Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*409T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.662T>C
  hgvsp: ENSP00000384747.2:p.Ile221Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.500T>C
  hgvsp: ENSP00000429394.1:p.Ile167Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.500T>C
  hgvsp: ENSP00000430833.1:p.Ile167Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.344T>C
  hgvsp: ENSP00000428305.1:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.344T>C
  hgvsp: ENSP00000429882.1:p.Ile115Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.170T>C
  hgvsp: ENSP00000429576.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*309T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.662T>C
  hgvsp: ENSP00000430493.1:p.Ile221Thr
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile221Thr
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

5-154252151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252151
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252151
    reference: chr 5
allele count: 1
allele frequency: 8.314625426124552e-6
allele num: 120270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.177G>A
  hgvsp: ENST00000524105.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.351G>A
  hgvsp: ENST00000521583.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.351G>A
  hgvsp: ENST00000520671.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*416G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.507G>A
  hgvsp: ENST00000519404.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.669G>A
  hgvsp: ENST00000517876.1:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.669G>A
  hgvsp: ENST00000403027.2:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.669G>A
  hgvsp: ENST00000285896.6:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.351G>A
  hgvsp: ENST00000523698.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*316G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.351G>A
  hgvsp: ENST00000521450.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.507G>A
  hgvsp: ENST00000518775.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg223Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

5-154252174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252174
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252174
    reference: chr 5
allele count: 1
allele frequency: 8.357849692431131e-6
allele num: 119648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.530C>T
  hgvsp: ENSP00000430833.1:p.Ser177Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.374C>T
  hgvsp: ENSP00000428565.1:p.Ser125Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.374C>T
  hgvsp: ENSP00000429882.1:p.Ser125Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.692C>T
  hgvsp: ENSP00000285896.6:p.Ser231Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.692C>T
  hgvsp: ENSP00000430493.1:p.Ser231Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.200C>T
  hgvsp: ENSP00000429576.1:p.Ser67Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.692C>T
  hgvsp: ENSP00000384747.2:p.Ser231Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*339C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.530C>T
  hgvsp: ENSP00000429394.1:p.Ser177Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*439C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.374C>T
  hgvsp: ENSP00000428305.1:p.Ser125Leu
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.374C>T
  hgvsp: ENSP00000431034.1:p.Ser125Leu
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser231Leu
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD

5-154252208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252208
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252208
    reference: chr 5
allele count: 1
allele frequency: 8.950628334109055e-6
allele num: 111724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.234A>G
  hgvsp: ENST00000524105.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428576
  ensembl transcript: ENST00000522644
  gene symbol: CNOT8
  hgvsc: ENST00000522644.1:c.*473A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.564A>G
  hgvsp: ENST00000519404.1:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.408A>G
  hgvsp: ENST00000521583.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.408A>G
  hgvsp: ENST00000523698.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.726A>G
  hgvsp: ENST00000285896.6:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.726A>G
  hgvsp: ENST00000517876.1:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*373A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.408A>G
  hgvsp: ENST00000521450.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.564A>G
  hgvsp: ENST00000518775.1:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.726A>G
  hgvsp: ENST00000403027.2:c.726A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.408A>G
  hgvsp: ENST00000520671.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys242Lys
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

5-154252224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252224
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252224
    reference: chr 5
allele count: 1
allele frequency: 9.523265337218826e-6
allele num: 105006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+13G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+13G>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

5-154252235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252235
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252235
    reference: chr 5
allele count: 2
allele frequency: 1.974996543756048e-5
allele num: 101266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+24C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+24C>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10575
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

5-154252237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252237
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252237
    reference: chr 5
allele count: 1
allele frequency: 9.967704636976197e-6
allele num: 100324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+26G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+26G>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22557
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

5-154252238-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252238
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252238
    reference: chr 5
allele count: 1
allele frequency: 9.956589270779402e-6
allele num: 100436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+27G>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+27G>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

5-154252244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252244
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252244
    reference: chr 5
allele count: 3
allele frequency: 3.073203712430085e-5
allele num: 97618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+33C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+33C>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11212
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22419
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5641
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

5-154252245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252245
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252245
    reference: chr 5
allele count: 337
allele frequency: 3.461736004108886e-3
allele num: 97350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+34G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+34G>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 2.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 22453
  bin: 1.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11386
  bin: 1.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 7802
  bin: 2.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.25e1
  variant carriers: 6
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

5-154252246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252246
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252246
    reference: chr 5
allele count: 1
allele frequency: 1.034489893033745e-5
allele num: 96666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+35G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+35G>A
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22266
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8940
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

5-154252249-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154252249
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154252249
    reference: chr 5
allele count: 1
allele frequency: 1.044735577425354e-5
allele num: 95718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.411+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.729+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.237+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*376+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.411+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.411+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.729+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.411+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.567+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.729+38G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.567+38G>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6347
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

5-154254800-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254800
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254800
    reference: chr 5
allele count: 1
allele frequency: 8.391937026904549e-6
allele num: 119162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.412-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*377-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.568-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.412-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.412-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.730-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.730-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.412-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.238-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.568-50T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.730-50T>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14087
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

5-154254806-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254806
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254806
    reference: chr 5
allele count: 1
allele frequency: 8.395177809866013e-6
allele num: 119116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.730-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.412-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.412-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*377-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.238-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.730-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.412-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.412-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.568-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.568-44C>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.730-44C>G
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

5-154254818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254818
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254818
    reference: chr 5
allele count: 15132
allele frequency: 1.26405479909782e-1
allele num: 119710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.568-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.568-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.730-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.412-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.730-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.238-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.412-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.730-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*377-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.412-32C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.412-32C>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 274
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 6.75e1
  variant carriers: 1164
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 485
genotype depth: GenotypeDepth
  all individuals: 21668
  bin: 2.75e1
  variant carriers: 355
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 6.25e1
  variant carriers: 1047
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 5.75e1
  variant carriers: 908
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.25e1
  variant carriers: 599
genotype depth: GenotypeDepth
  all individuals: 8560
  bin: 3.25e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 745
genotype depth: GenotypeDepth
  all individuals: 10569
  bin: 2.25e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.25e1
  variant carriers: 1244
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 8.25e1
  variant carriers: 1027
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 7.75e1
  variant carriers: 1149
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.75e1
  variant carriers: 402
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 8.75e1
  variant carriers: 762
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 9.75e1
  variant carriers: 2459
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 3
num of homozygotes: 1230
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

5-154254830-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254830
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254830
    reference: chr 5
allele count: 1
allele frequency: 8.321959988016378e-6
allele num: 120164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.412-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.568-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.730-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.238-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*377-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.730-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.412-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.412-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.412-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.568-20T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.730-20T>C
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13534
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

5-154254850-TTGTTTTTTGAGGACAGCATTGATGATGCCAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254850
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254819
    reference: chr 5
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsp: ENSP00000430833.1:p.Leu190CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsp: ENSP00000428565.1:p.Leu138CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsp: ENSP00000431034.1:p.Leu138CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsp: ENSP00000285896.6:p.Leu244CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsp: ENSP00000429394.1:p.Leu190CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsp: ENSP00000429576.1:p.Leu80CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsp: ENSP00000430493.1:p.Leu244CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsp: ENSP00000429882.1:p.Leu138CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsp: ENSP00000384747.2:p.Leu244CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsp: ENSP00000428305.1:p.Leu138CysfsTer9
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu244CysfsTer9
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: TTGTTTTTTGAGGACAGCATTGATGATGCCAA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

5-154254877-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254877
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254877
    reference: chr 5
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.439G>T
  hgvsp: ENSP00000429882.1:p.Ala147Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.439G>T
  hgvsp: ENSP00000431034.1:p.Ala147Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.439G>T
  hgvsp: ENSP00000428565.1:p.Ala147Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.757G>T
  hgvsp: ENSP00000285896.6:p.Ala253Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.757G>T
  hgvsp: ENSP00000430493.1:p.Ala253Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.595G>T
  hgvsp: ENSP00000429394.1:p.Ala199Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.757G>T
  hgvsp: ENSP00000384747.2:p.Ala253Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.595G>T
  hgvsp: ENSP00000430833.1:p.Ala199Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.265G>T
  hgvsp: ENSP00000429576.1:p.Ala89Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.439G>T
  hgvsp: ENSP00000428305.1:p.Ala147Ser
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*404G>T
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala253Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-154254878-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254878
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254878
    reference: chr 5
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.266C>T
  hgvsp: ENSP00000429576.1:p.Ala89Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.440C>T
  hgvsp: ENSP00000431034.1:p.Ala147Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.758C>T
  hgvsp: ENSP00000285896.6:p.Ala253Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.440C>T
  hgvsp: ENSP00000428305.1:p.Ala147Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*405C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.440C>T
  hgvsp: ENSP00000428565.1:p.Ala147Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.596C>T
  hgvsp: ENSP00000430833.1:p.Ala199Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.440C>T
  hgvsp: ENSP00000429882.1:p.Ala147Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.758C>T
  hgvsp: ENSP00000384747.2:p.Ala253Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.596C>T
  hgvsp: ENSP00000429394.1:p.Ala199Val
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.758C>T
  hgvsp: ENSP00000430493.1:p.Ala253Val
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28811
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala253Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

5-154254881-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254881
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254881
    reference: chr 5
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.761A>G
  hgvsp: ENSP00000285896.6:p.Lys254Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.761A>G
  hgvsp: ENSP00000384747.2:p.Lys254Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.269A>G
  hgvsp: ENSP00000429576.1:p.Lys90Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.443A>G
  hgvsp: ENSP00000428565.1:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.443A>G
  hgvsp: ENSP00000429882.1:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.761A>G
  hgvsp: ENSP00000430493.1:p.Lys254Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.443A>G
  hgvsp: ENSP00000431034.1:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.599A>G
  hgvsp: ENSP00000430833.1:p.Lys200Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.443A>G
  hgvsp: ENSP00000428305.1:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*408A>G
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.599A>G
  hgvsp: ENSP00000429394.1:p.Lys200Arg
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys254Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

5-154254886-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254886
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254886
    reference: chr 5
allele count: 2
allele frequency: 1.649838315845047e-5
allele num: 121224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*413T>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.274T>C
  hgvsp: ENSP00000429576.1:p.Cys92Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.604T>C
  hgvsp: ENSP00000430833.1:p.Cys202Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.448T>C
  hgvsp: ENSP00000428305.1:p.Cys150Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.766T>C
  hgvsp: ENSP00000384747.2:p.Cys256Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.448T>C
  hgvsp: ENSP00000431034.1:p.Cys150Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.604T>C
  hgvsp: ENSP00000429394.1:p.Cys202Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.448T>C
  hgvsp: ENSP00000429882.1:p.Cys150Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.766T>C
  hgvsp: ENSP00000285896.6:p.Cys256Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.766T>C
  hgvsp: ENSP00000430493.1:p.Cys256Arg
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.448T>C
  hgvsp: ENSP00000428565.1:p.Cys150Arg
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys256Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

5-154254903-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254903
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254903
    reference: chr 5
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.465C>T
  hgvsp: ENST00000520671.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.783C>T
  hgvsp: ENST00000403027.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.621C>T
  hgvsp: ENST00000519404.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.465C>T
  hgvsp: ENST00000521583.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.291C>T
  hgvsp: ENST00000524105.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.621C>T
  hgvsp: ENST00000518775.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.783C>T
  hgvsp: ENST00000285896.6:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.465C>T
  hgvsp: ENST00000521450.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.783C>T
  hgvsp: ENST00000517876.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*430C>T
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.465C>T
  hgvsp: ENST00000523698.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly261Gly
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS

5-154254918-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254918
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254918
    reference: chr 5
allele count: 69
allele frequency: 5.686500741717488e-4
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*445G>C
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.480G>C
  hgvsp: ENST00000521583.1:c.480G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.480G>C
  hgvsp: ENST00000520671.1:c.480G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.636G>C
  hgvsp: ENST00000519404.1:c.636G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.480G>C
  hgvsp: ENST00000523698.1:c.480G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.306G>C
  hgvsp: ENST00000524105.1:c.306G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.798G>C
  hgvsp: ENST00000517876.1:c.798G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.798G>C
  hgvsp: ENST00000403027.2:c.798G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.798G>C
  hgvsp: ENST00000285896.6:c.798G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.480G>C
  hgvsp: ENST00000521450.1:c.480G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.636G>C
  hgvsp: ENST00000518775.1:c.636G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 28894
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
hgvs: p.Val266Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

5-154254927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254927
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254927
    reference: chr 5
allele count: 9
allele frequency: 7.417174880501072e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.807G>A
  hgvsp: ENST00000285896.6:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.807G>A
  hgvsp: ENST00000517876.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.489G>A
  hgvsp: ENST00000520671.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.807G>A
  hgvsp: ENST00000403027.2:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.645G>A
  hgvsp: ENST00000519404.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.489G>A
  hgvsp: ENST00000521450.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.315G>A
  hgvsp: ENST00000524105.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*454G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.489G>A
  hgvsp: ENST00000523698.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.645G>A
  hgvsp: ENST00000518775.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.489G>A
  hgvsp: ENST00000521583.1:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Lys269Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

5-154254940-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 154254940
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 154254940
    reference: chr 5
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430493
  ensembl transcript: ENST00000517876
  gene symbol: CNOT8
  hgvsc: ENST00000517876.1:c.820G>A
  hgvsp: ENSP00000430493.1:p.Val274Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429394
  ensembl transcript: ENST00000518775
  gene symbol: CNOT8
  hgvsc: ENST00000518775.1:c.658G>A
  hgvsp: ENSP00000429394.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428565
  ensembl transcript: ENST00000523698
  gene symbol: CNOT8
  hgvsc: ENST00000523698.1:c.502G>A
  hgvsp: ENSP00000428565.1:p.Val168Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429882
  ensembl transcript: ENST00000521583
  gene symbol: CNOT8
  hgvsc: ENST00000521583.1:c.502G>A
  hgvsp: ENSP00000429882.1:p.Val168Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000429576
  ensembl transcript: ENST00000524105
  gene symbol: CNOT8
  hgvsc: ENST00000524105.1:c.328G>A
  hgvsp: ENSP00000429576.1:p.Val110Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428600
  ensembl transcript: ENST00000521729
  gene symbol: CNOT8
  hgvsc: ENST00000521729.1:c.*467G>A
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000428305
  ensembl transcript: ENST00000520671
  gene symbol: CNOT8
  hgvsc: ENST00000520671.1:c.502G>A
  hgvsp: ENSP00000428305.1:p.Val168Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000430833
  ensembl transcript: ENST00000519404
  gene symbol: CNOT8
  hgvsc: ENST00000519404.1:c.658G>A
  hgvsp: ENSP00000430833.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000285896
  ensembl transcript: ENST00000285896
  gene symbol: CNOT8
  hgvsc: ENST00000285896.6:c.820G>A
  hgvsp: ENSP00000285896.6:p.Val274Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000431034
  ensembl transcript: ENST00000521450
  gene symbol: CNOT8
  hgvsc: ENST00000521450.1:c.502G>A
  hgvsp: ENSP00000431034.1:p.Val168Met
  variant of: http://identifiers.org/hgnc/9207
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155508
  ensembl protein: ENSP00000384747
  ensembl transcript: ENST00000403027
  gene symbol: CNOT8
  hgvsc: ENST00000403027.2:c.820G>A
  hgvsp: ENSP00000384747.2:p.Val274Met
  variant of: http://identifiers.org/hgnc/9207
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val274Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum

GenotypeDepth
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16554
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1340
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7997
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 391
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3730
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.0790273556231e-5
allele num: 16450
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.893e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.198e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.782e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.295e0

DP
type: SiteQuality
SIO_000300: 1.83467e6

GenotypeDepth
all individuals: 7958
bin: 3.25e1
variant carriers: 6

GenotypeDepth
all individuals: 629
bin: 4.25e1
variant carriers: 25

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16556
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 270
bin: 5.25e1
variant carriers: 25

GenotypeDepth
all individuals: 1267
bin: 9.75e1
variant carriers: 15

GenotypeDepth
all individuals: 207
bin: 6.25e1
variant carriers: 19

GenotypeQuality
all individuals: 297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3828
bin: 9.75e1
variant carriers: 187

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44460
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 378
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 163
allele frequency: 2.447006545367201e-3
allele num: 66612
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.890173410404624e-4
allele num: 10380
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 21
allele frequency: 3.177004538577912e-3
allele num: 6610
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.839128e6

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 1.408e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeDepth
all individuals: 30520
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1310
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 176
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 871
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

FS
type: SiteQuality
SIO_000300: 1.087e0

MQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.26e-1

DP
type: SiteQuality
SIO_000300: 1.833554e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.011e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1256
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 178
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30573
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3646
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7137
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
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African
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Latino
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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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East Asian
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MQRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
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BaseQRankSum
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SIO_000300: 3.2e-2

ReadPosRankSum
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ClippingRankSum
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SIO_000300: -2.559e0

DP
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SIO_000300: 1.836442e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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num of homozygotes: 0

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

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

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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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

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

MQRankSum
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SIO_000300: 4.53e-1

QD
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BaseQRankSum
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DP
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.818e1

ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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SIO_000300: -8.48e-1

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

African
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allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

Latino
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allele count: 8
allele frequency: 6.926406926406926e-4
allele num: 11550
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.83349e6

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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QD
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MQRankSum
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ClippingRankSum
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SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeDepth
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variant carriers: 0

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

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

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

Other
type: Population
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

MQ
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SIO_000300: 3.69e1

ClippingRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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SIO_000300: -2.264e0

ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66246
num of homozygotes: 0

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

BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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FS
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 900
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 6.105751618024179e-5
allele num: 16378
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.165988407941794e-5
allele num: 16218
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.547221190741428e-5
allele num: 64632
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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FS
type: SiteQuality
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QD
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.590786166523496e-5
allele num: 62862
num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

MQRankSum
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SIO_000300: -9.66e-1

QD
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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SIO_000300: 2.02e0

ReadPosRankSum
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SIO_000300: 1.08e0

DP
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SIO_000300: 1.725871e6

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15076
num of homozygotes: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.345532831001076e-4
allele num: 7432
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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SIO_000300: 1.52e-1

ReadPosRankSum
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SIO_000300: 1.58e0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 13
allele frequency: 2.40580353838182e-4
allele num: 54036
num of homozygotes: 0

Latino
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allele frequency: 4.222081486172683e-4
allele num: 9474
num of homozygotes: 0

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

East Asian
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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

Other
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MQ
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SIO_000300: 5.943e1

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9440
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.07342206955775e-4
allele num: 9316
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.812137846904544e-5
allele num: 52464
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.283712784588441e-4
allele num: 9136
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.411233418007338e-4
allele num: 7086
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 3.77e0

QD
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SIO_000300: 1.415e1

InbreedingCoeff
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SIO_000300: -4.9e-3

DP
type: SiteQuality
SIO_000300: 1.225227e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.31e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8882
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.928655614048873e-5
allele num: 50908
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.881365262868153e-5
allele num: 14532
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
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MQRankSum
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ClippingRankSum
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SIO_000300: -9.96e-1

MQ
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FS
type: SiteQuality
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VQSLOD
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SIO_000300: 1.03e0

InbreedingCoeff
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SIO_000300: -5.7e-3

DP
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SIO_000300: 1.193206e6

QD
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SIO_000300: 1.362e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 28

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8818
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6882
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50640
num of homozygotes: 0

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

South Asian
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allele count: 31
allele frequency: 2.142067440574903e-3
allele num: 14472
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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MQ
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SIO_000300: 6.0e1

DP
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BaseQRankSum
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SIO_000300: 1.03e0

MQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 6.6e-3

ReadPosRankSum
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SIO_000300: 2.99e-1

ClippingRankSum
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SIO_000300: -2.67e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6882
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8818
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 2.072968490878939e-4
allele num: 14472
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 6.6e-3

ReadPosRankSum
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BaseQRankSum
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DP
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QD
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VQSLOD
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MQRankSum
type: SiteQuality
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MQ
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -2.67e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49734
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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Other
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VQSLOD
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QD
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DP
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BaseQRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele num: 8314
num of homozygotes: 0

Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
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FS
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.611343860779891e-4
allele num: 6206
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

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

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

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

South Asian
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European (Non-Finnish)
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African
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East Asian
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Latino
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Other
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BaseQRankSum
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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European (Non-Finnish)
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Other
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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QD
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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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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bin: 3.25e1
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 3.866228494104001e-4
allele num: 10346
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 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

DP
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511715797430083e-5
allele num: 66150
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -1.623e0

ReadPosRankSum
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MQ
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ClippingRankSum
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DP
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FS
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VQSLOD
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MQRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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South Asian
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65800
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 6.5e-1

DP
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SIO_000300: 1.585191e6

QD
type: SiteQuality
SIO_000300: 1.006e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 61768
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Latino
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Other
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 9.07e-1

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.052e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.716856093122274e-5
allele num: 58246
num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 56308
num of homozygotes: 0

European (Finnish)
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African
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Latino
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Other
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East Asian
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 13626
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5568
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.469723691945914e-4
allele num: 6804
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
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QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -2.39e-1

DP
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5454
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Latino
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allele frequency: 0.0e0
allele num: 8702
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.837965005146302e-5
allele num: 54408
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.554011179936546e-5
allele num: 13238
num of homozygotes: 0

FS
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 333

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 9
allele frequency: 1.060570351166627e-3
allele num: 8486
num of homozygotes: 0

European (Finnish)
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allele count: 23
allele frequency: 4.217088375504217e-3
allele num: 5454
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 25
allele frequency: 2.895529302756544e-3
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 262
allele frequency: 4.831808793154323e-3
allele num: 54224
num of homozygotes: 0

South Asian
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allele count: 12
allele frequency: 9.052504526252263e-4
allele num: 13256
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Other
type: Population
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allele frequency: 7.751937984496124e-3
allele num: 774
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VQSLOD
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SIO_000300: 6.48e0

BaseQRankSum
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DP
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QD
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ClippingRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

FS
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MQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

DP
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SIO_000300: 1.112771e6

ReadPosRankSum
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.29e-1

BaseQRankSum
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SIO_000300: -2.637e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13098
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.877088260690017e-5
allele num: 53274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5386
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VQSLOD
type: SiteQuality
SIO_000300: -7.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
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DP
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FS
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InbreedingCoeff
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SIO_000300: -3.3e-3

ReadPosRankSum
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SIO_000300: -9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.715e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521884702014975e-5
allele num: 65708
num of homozygotes: 0

European (Finnish)
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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: 8612
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
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VQSLOD
type: SiteQuality
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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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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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522533495736906e-5
allele num: 65680
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -5.245e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16684
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GenotypeQuality
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variant carriers: 30

European (Finnish)
type: Population
allele count: 833
allele frequency: 1.260593220338983e-1
allele num: 6608
num of homozygotes: 51

East Asian
type: Population
allele count: 717
allele frequency: 8.3197957762822e-2
allele num: 8618
num of homozygotes: 35

African
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allele count: 3203
allele frequency: 3.1334376834279e-1
allele num: 10222
num of homozygotes: 498

South Asian
type: Population
allele count: 1982
allele frequency: 1.244037157921165e-1
allele num: 15932
num of homozygotes: 141

Latino
type: Population
allele count: 2601
allele frequency: 2.257420586703697e-1
allele num: 11522
num of homozygotes: 266

Other
type: Population
allele count: 105
allele frequency: 1.171875e-1
allele num: 896
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 5691
allele frequency: 8.634239592183518e-2
allele num: 65912
num of homozygotes: 236

QD
type: SiteQuality
SIO_000300: 1.407e1

FS
type: SiteQuality
SIO_000300: 1.369e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.998e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

VQSLOD
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SIO_000300: 5.18e0

MQRankSum
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SIO_000300: 1.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.66e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 2.386709e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66070
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

South Asian
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allele frequency: 6.187353050365054e-5
allele num: 16162
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11544
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
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SIO_000300: 3.92e0

DP
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SIO_000300: 1.794231e6

InbreedingCoeff
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SIO_000300: 1.1e-3

MQ
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SIO_000300: 6.0e1

VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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SIO_000300: -1.945e0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 2.21e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66316
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 1.63e-2

MQRankSum
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SIO_000300: 1.02e0

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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FS
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SIO_000300: 4.824e0

DP
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SIO_000300: 1.807218e6

MQ
type: SiteQuality
SIO_000300: 5.755e1

QD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

Latino
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allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.813341e6

BaseQRankSum
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SIO_000300: -9.61e-1

FS
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SIO_000300: 2.93e0

MQ
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SIO_000300: 5.956e1

MQRankSum
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QD
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ClippingRankSum
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SIO_000300: 6.21e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: 2.49e-2

ReadPosRankSum
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SIO_000300: -1.563e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 3.75e1
variant carriers: 0

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

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

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.813487e6

MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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SIO_000300: -2.191e0

MQRankSum
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SIO_000300: -6.45e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 11566
num of homozygotes: 0

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

African
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allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 9471
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2799
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4071
bin: 9.75e1
variant carriers: 69

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

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

GenotypeQuality
all individuals: 632
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2644
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38888
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.457814661134163e-4
allele num: 11568
num of homozygotes: 0

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

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

African
type: Population
allele count: 64
allele frequency: 6.160954948016942e-3
allele num: 10388
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.814e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

FS
type: SiteQuality
SIO_000300: 1.169e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

QD
type: SiteQuality
SIO_000300: 1.079e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

DP
type: SiteQuality
SIO_000300: 1.81575e6

GenotypeDepth
all individuals: 249
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 633
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2645
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4004
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2799
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9468
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38939
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.778738115816768e-4
allele num: 11570
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.93e-1

DP
type: SiteQuality
SIO_000300: 1.812347e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.277e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

GenotypeDepth
all individuals: 333
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38920
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2794
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3989
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 632
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.798e0