8-17100456-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100456
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100455
    reference: chr 8
allele count: 8342
allele frequency: 1.447509977442304e-1
allele num: 57630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+44delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.255delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+44delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+44delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+44delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+44delT
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 7.5e0
  variant carriers: 496
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17380
  bin: 1.25e1
  variant carriers: 2388
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 1037
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 1.75e1
  variant carriers: 3139
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 417
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 2064
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 282
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 807
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 728
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 635
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 5.25e1
  variant carriers: 713
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 372
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 484
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 355
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 431
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 8.75e1
  variant carriers: 190
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 734
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 7.25e1
  variant carriers: 346
genotype quality: GenotypeQuality
  all individuals: 19754
  bin: 2.5e0
  variant carriers: 512
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: GA
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

8-17100456-G-GAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100456
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100458
    reference: chr 8
allele count: 1179
allele frequency: 2.045809474232171e-2
allele num: 57630
alternate allele: GAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.254_255dupTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+43_*259+44dupTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+43_311+44dupTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+43_311+44dupTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+43_311+44dupTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+43_250+44dupTT
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17380
  bin: 1.25e1
  variant carriers: 861
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 1.75e1
  variant carriers: 513
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 7.5e0
  variant carriers: 486
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 8.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 9.75e1
  variant carriers: 204
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 141
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 109
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 5.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 116
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 19754
  bin: 2.5e0
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 1.75e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 148
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 5.25e1
  variant carriers: 103
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-17100456-G-GAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100456
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100459
    reference: chr 8
allele count: 47
allele frequency: 8.155474579212216e-4
allele num: 57630
alternate allele: GAAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.253_255dupTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+42_250+44dupTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+42_*259+44dupTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+42_311+44dupTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+42_311+44dupTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+42_311+44dupTTT
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17380
  bin: 1.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 19754
  bin: 2.5e0
  variant carriers: 6
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

8-17100456-G-GAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100456
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100460
    reference: chr 8
allele count: 3
allele frequency: 5.205622071837585e-5
allele num: 57630
alternate allele: GAAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+41_250+44dupTTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+41_311+44dupTTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.252_255dupTTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+41_311+44dupTTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+41_311+44dupTTTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+41_*259+44dupTTTT
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17380
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19754
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-17100456-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100456
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100454
    reference: chr 8
allele count: 147
allele frequency: 2.550754815200416e-3
allele num: 57630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.254_255delTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+43_311+44delTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+43_250+44delTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+43_311+44delTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+43_*259+44delTT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+43_311+44delTT
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 1.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17380
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 5.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 2.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 19754
  bin: 2.5e0
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 2598
  bin: 7.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 5.25e1
  variant carriers: 11
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: GAA
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP

8-17100457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100457
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100457
    reference: chr 8
allele count: 3
allele frequency: 1.368613138686131e-3
allele num: 2192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+44T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+44T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+44T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+44T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.255T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+44T>C
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9184
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31857
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

8-17100458-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100458
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100458
    reference: chr 8
allele count: 1
allele frequency: 2.58384579608289e-5
allele num: 38702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+43T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+43T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+43T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+43T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+43T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.254T>C
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9019
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2468
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2656
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3326
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27418
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

8-17100459-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100459
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100459
    reference: chr 8
allele count: 1
allele frequency: 1.030821564787135e-5
allele num: 97010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+42T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.253T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+42T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+42T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+42T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+42T>C
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9574
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6938
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4076
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2349
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8193
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5865
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

8-17100474-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100474
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100474
    reference: chr 8
allele count: 4
allele frequency: 3.5331943610218e-5
allele num: 113212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.238A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2492
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

8-17100477-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100477
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100477
    reference: chr 8
allele count: 23
allele frequency: 2.009927293064877e-4
allele num: 114432
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+24C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+24C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+24C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+24C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.235C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+24C>A
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22853
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 9.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

8-17100483-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100483
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100483
    reference: chr 8
allele count: 1
allele frequency: 8.564136820649846e-6
allele num: 116766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+18G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+18G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+18G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.229G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+18G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+18G>C
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16666
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35850
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2824
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8045
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2732
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

8-17100489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100489
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100489
    reference: chr 8
allele count: 4
allele frequency: 3.381577167590964e-5
allele num: 118288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311+12A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.223A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311+12A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311+12A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259+12A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250+12A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17458
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6859
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8581
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37641
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

8-17100501-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100501
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100501
    reference: chr 8
allele count: 3
allele frequency: 2.510082163356147e-5
allele num: 119518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.311C>T
  hgvsp: ENSP00000429093.1:p.Thr104Met
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.250C>T
  hgvsp: ENSP00000428147.1:p.Thr84Met
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*259C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.311C>T
  hgvsp: ENSP00000355279.4:p.Thr104Met
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.311C>T
  hgvsp: ENSP00000430160.1:p.Thr104Met
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.211C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17913
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8698
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38532
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr104Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

8-17100512-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100512
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100512
    reference: chr 8
allele count: 1
allele frequency: 8.334583520861462e-6
allele num: 119982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.300A>G
  hgvsp: ENST00000524358.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*248A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*292A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.300A>G
  hgvsp: ENST00000361272.4:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.300A>G
  hgvsp: ENST00000523917.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.200A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.239A>G
  hgvsp: ENST00000519918.1:c.239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys100Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-17100548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100548
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100548
    reference: chr 8
allele count: 2
allele frequency: 1.655053706492776e-5
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.264C>T
  hgvsp: ENST00000523917.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.164C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.264C>T
  hgvsp: ENST00000524358.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.264C>T
  hgvsp: ENST00000361272.4:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.203C>T
  hgvsp: ENST00000519918.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*212C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*256C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39269
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr88Tyr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

8-17100550-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100550
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100550
    reference: chr 8
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.162T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.262T>C
  hgvsp: ENSP00000355279.4:p.Tyr88His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.262T>C
  hgvsp: ENSP00000429093.1:p.Tyr88His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.262T>C
  hgvsp: ENSP00000430160.1:p.Tyr88His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*210T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.201T>C
  hgvsp: ENSP00000428147.1:p.Tyr68His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*254T>C
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8781
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr88His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-17100552-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100552
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100552
    reference: chr 8
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.260A>T
  hgvsp: ENSP00000355279.4:p.Glu87Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.160A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*252A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.260A>T
  hgvsp: ENSP00000430160.1:p.Glu87Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.260A>T
  hgvsp: ENSP00000429093.1:p.Glu87Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.199A>T
  hgvsp: ENSP00000428147.1:p.Glu67Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*208A>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu87Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

8-17100553-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100553
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100553
    reference: chr 8
allele count: 8
allele frequency: 6.617038875103391e-5
allele num: 120900
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.159G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*251G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.259G>C
  hgvsp: ENSP00000355279.4:p.Glu87Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*207G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.198G>C
  hgvsp: ENSP00000428147.1:p.Glu67Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.259G>C
  hgvsp: ENSP00000429093.1:p.Glu87Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.259G>C
  hgvsp: ENSP00000430160.1:p.Glu87Gln
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39329
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu87Gln
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

8-17100555-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100555
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100555
    reference: chr 8
allele count: 1
allele frequency: 8.268973158913126e-6
allele num: 120934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*249G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.257G>C
  hgvsp: ENSP00000355279.4:p.Gly86Ala
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.257G>C
  hgvsp: ENSP00000430160.1:p.Gly86Ala
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.157G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.196G>C
  hgvsp: ENSP00000428147.1:p.Gly66Ala
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*205G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.257G>C
  hgvsp: ENSP00000429093.1:p.Gly86Ala
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly86Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

8-17100559-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100559
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100559
    reference: chr 8
allele count: 1
allele frequency: 8.265692417053776e-6
allele num: 120982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.253C>A
  hgvsp: ENSP00000429093.1:p.Gln85Lys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.253C>A
  hgvsp: ENSP00000430160.1:p.Gln85Lys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*245C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.253C>A
  hgvsp: ENSP00000355279.4:p.Gln85Lys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.192C>A
  hgvsp: ENSP00000428147.1:p.Gln65Lys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*201C>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.153C>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8782
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln85Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-17100565-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100565
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100565
    reference: chr 8
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.247A>C
  hgvsp: ENSP00000429093.1:p.Asn83His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.247A>C
  hgvsp: ENSP00000355279.4:p.Asn83His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.147A>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*195A>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.247A>C
  hgvsp: ENSP00000430160.1:p.Asn83His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*239A>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.186A>C
  hgvsp: ENSP00000428147.1:p.Asn63His
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn83His
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

8-17100568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100568
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100568
    reference: chr 8
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*236A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.183A>G
  hgvsp: ENSP00000428147.1:p.Met62Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.244A>G
  hgvsp: ENSP00000430160.1:p.Met82Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.244A>G
  hgvsp: ENSP00000429093.1:p.Met82Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.244A>G
  hgvsp: ENSP00000355279.4:p.Met82Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*192A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.144A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8786
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39451
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met82Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

8-17100573-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100573
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100573
    reference: chr 8
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.178C>T
  hgvsp: ENSP00000428147.1:p.Thr60Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.239C>T
  hgvsp: ENSP00000430160.1:p.Thr80Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*231C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.239C>T
  hgvsp: ENSP00000355279.4:p.Thr80Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.139C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.239C>T
  hgvsp: ENSP00000429093.1:p.Thr80Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*187C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr80Ile
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

8-17100584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100584
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100584
    reference: chr 8
allele count: 2
allele frequency: 1.650273945474949e-5
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.167G>A
  hgvsp: ENST00000519918.1:c.167G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.228G>A
  hgvsp: ENST00000361272.4:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*220G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.128G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.228G>A
  hgvsp: ENST00000524358.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.228G>A
  hgvsp: ENST00000523917.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8788
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln76Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

8-17100598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100598
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100598
    reference: chr 8
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.153T>C
  hgvsp: ENST00000519918.1:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*162T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.214T>C
  hgvsp: ENST00000523917.1:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.114T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.214T>C
  hgvsp: ENST00000524358.1:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*206T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.214T>C
  hgvsp: ENST00000361272.4:c.214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39501
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu72Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

8-17100619-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100619
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100619
    reference: chr 8
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.193T>C
  hgvsp: ENST00000361272.4:c.193T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*141T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*185T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.193T>C
  hgvsp: ENST00000524358.1:c.193T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.93T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.132T>C
  hgvsp: ENST00000519918.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.193T>C
  hgvsp: ENST00000523917.1:c.193T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3014
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu65Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

8-17100623-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100623
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100623
    reference: chr 8
allele count: 4
allele frequency: 3.298207424264912e-5
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*181A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.128A>G
  hgvsp: ENST00000519918.1:c.128A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.189A>G
  hgvsp: ENST00000361272.4:c.189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*137A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.189A>G
  hgvsp: ENST00000524358.1:c.189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.189A>G
  hgvsp: ENST00000523917.1:c.189A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.89A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln63Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

8-17100629-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100629
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100629
    reference: chr 8
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.122A>G
  hgvsp: ENST00000519918.1:c.122A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*131A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*175A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.183A>G
  hgvsp: ENST00000523917.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.83A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.183A>G
  hgvsp: ENST00000361272.4:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.183A>G
  hgvsp: ENST00000524358.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln61Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

8-17100630-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100630
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100630
    reference: chr 8
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.182A>G
  hgvsp: ENSP00000355279.4:p.Gln61Arg
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.82A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.121A>G
  hgvsp: ENSP00000428147.1:p.Gln41Arg
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*174A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.182A>G
  hgvsp: ENSP00000429093.1:p.Gln61Arg
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*130A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.182A>G
  hgvsp: ENSP00000430160.1:p.Gln61Arg
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39627
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln61Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

8-17100689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100689
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100689
    reference: chr 8
allele count: 3
allele frequency: 2.511426992817319e-5
allele num: 119454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*71C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.123C>T
  hgvsp: ENST00000524358.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.62C>T
  hgvsp: ENST00000519918.1:c.62C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.123C>T
  hgvsp: ENST00000361272.4:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.123C>T
  hgvsp: ENST00000523917.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.23C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*115C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27697
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8505
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr41Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-17100698-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100698
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100698
    reference: chr 8
allele count: 1
allele frequency: 8.436255652291287e-6
allele num: 118536
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-4A>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-4A>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16803
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 3.25e1
  variant carriers: 0
hgvs: c.118-4A>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

8-17100703-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100703
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100703
    reference: chr 8
allele count: 1
allele frequency: 8.460952703274388e-6
allele num: 118190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-9A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-9A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27336
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-17100707-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100707
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100707
    reference: chr 8
allele count: 1
allele frequency: 8.482915408367548e-6
allele num: 117884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-13A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-13A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2898
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8271
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-17100711-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100711
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100711
    reference: chr 8
allele count: 1
allele frequency: 8.507597284374947e-6
allele num: 117542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-17T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-17T>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS

8-17100712-GATTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100712
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100708
    reference: chr 8
allele count: 13
allele frequency: 1.107287656297911e-4
allele num: 117404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-22_*66-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-22_*110-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-22_118-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-22_118-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-22_57-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-22_118-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-22_118-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-22_18-19delGAAT
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26737
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15828
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34661
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 9.75e1
  variant carriers: 13
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: GATTC
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

8-17100714-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100714
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100714
    reference: chr 8
allele count: 1
allele frequency: 8.527766407422568e-6
allele num: 117264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-20A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-20A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

8-17100721-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100721
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100721
    reference: chr 8
allele count: 6
allele frequency: 5.140154890000685e-5
allele num: 116728
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-27A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-27A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-17100723-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100723
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100723
    reference: chr 8
allele count: 1
allele frequency: 8.587081594449311e-6
allele num: 116454
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-29A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-29A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2904
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

8-17100726-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100726
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100725
    reference: chr 8
allele count: 1
allele frequency: 8.606148232297153e-6
allele num: 116196
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-33delT
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-33delT
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1823
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2951
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: TA
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/8-17100727-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100727
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100727
    reference: chr 8
allele count: 1
allele frequency: 8.632596685082874e-6
allele num: 115840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-33T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-33T>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2903
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

8-17100727-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100727
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100727
    reference: chr 8
allele count: 1
allele frequency: 8.632596685082874e-6
allele num: 115840
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-33T>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-33T>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15324
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

8-17100732-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100732
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100732
    reference: chr 8
allele count: 1
allele frequency: 8.650519031141869e-6
allele num: 115600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-38C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-38C>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7912
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

8-17100742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100742
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100742
    reference: chr 8
allele count: 1
allele frequency: 8.775008775008775e-6
allele num: 113960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-48G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-48G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-17100743-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100743
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100743
    reference: chr 8
allele count: 1
allele frequency: 8.761631065239105e-6
allele num: 114134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-49T>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-49T>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25980
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

8-17100745-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100745
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100745
    reference: chr 8
allele count: 4
allele frequency: 3.522367030644593e-5
allele num: 113560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-51A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-51A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16013
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22994
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7223
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2649
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/8-17100746-CCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100746
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100744
    reference: chr 8
allele count: 1
allele frequency: 8.808865241979528e-6
allele num: 113522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-54_118-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-54_57-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-54_118-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-54_118-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-54_18-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-54_118-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*66-54_*66-53delTG
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*110-54_*110-53delTG
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: CCA
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

8-17100969-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100969
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100969
    reference: chr 8
allele count: 119
allele frequency: 1.089344562431344e-2
allele num: 10924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*91C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-275C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-275C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-275C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-275C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-275C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-275C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 2.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4241
  bin: 9.75e1
  variant carriers: 119
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.25e1
  variant carriers: 2
num of homozygotes: 1
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-17100977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100977
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100977
    reference: chr 8
allele count: 4
allele frequency: 3.677146534289392e-4
allele num: 10878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-283G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-283G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*83G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-283G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-283G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-283G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-283G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4198
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-17100994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17100994
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17100994
    reference: chr 8
allele count: 1
allele frequency: 9.233610341643582e-5
allele num: 10830
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-300G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.*66G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-300G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-300G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-300G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-300G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-300G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

8-17101119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17101119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17101119
    reference: chr 8
allele count: 6
allele frequency: 5.572065378900445e-4
allele num: 10768
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-425G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-425G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.118-65G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.130G>A
  hgvsp: ENSP00000428783.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-425G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-425G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-425G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-425G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu44Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-17101132-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17101132
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17101132
    reference: chr 8
allele count: 2
allele frequency: 1.857700167193015e-4
allele num: 10766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-438G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-438G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-438G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.118-1G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-438G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-438G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-438G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.118-78G>C
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4196
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
hgvs: c.118-1G>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

8-17101147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17101147
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17101147
    reference: chr 8
allele count: 1
allele frequency: 9.29022668153103e-5
allele num: 10764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-453A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-453A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-453A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-453A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.118-16A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-453A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-453A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.118-93A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

8-17101151-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17101151
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17101151
    reference: chr 8
allele count: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-457G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-457G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.118-20G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-457G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-457G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.118-97G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-457G>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-457G>C
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/8-17101162-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17101162
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17101162
    reference: chr 8
allele count: 1
allele frequency: 9.286775631500742e-5
allele num: 10768
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.118-468G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.118-468G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.57-468G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.118-468G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.118-108G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.118-468G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.118-31G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.18-468G>T
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

8-17102498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102498
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102498
    reference: chr 8
allele count: 1
allele frequency: 8.342370901810295e-6
allele num: 119870
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+47A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.450A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+47A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

8-17102504-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102504
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102504
    reference: chr 8
allele count: 1
allele frequency: 8.340144451301897e-6
allele num: 119902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.444G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+41G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+41G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

8-17102510-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102510
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102510
    reference: chr 8
allele count: 12
allele frequency: 9.996334677284996e-5
allele num: 120044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.438A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+35A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+35A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

8-17102513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102513
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102513
    reference: chr 8
allele count: 2
allele frequency: 1.6655008160954e-5
allele num: 120084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.435C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+32C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+32C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

8-17102515-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102515
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102515
    reference: chr 8
allele count: 3
allele frequency: 2.496671105193076e-5
allele num: 120160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.433T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+30T>C
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+30T>C
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-17102517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102517
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102517
    reference: chr 8
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+28G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.431G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+28G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

8-17102518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102518
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102518
    reference: chr 8
allele count: 2
allele frequency: 1.662703889064397e-5
allele num: 120286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.430C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+27C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+27C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4304
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-17102518-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102518
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102518
    reference: chr 8
allele count: 2
allele frequency: 1.662703889064397e-5
allele num: 120286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.430C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+27C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+27C>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

8-17102530-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102530
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102530
    reference: chr 8
allele count: 2
allele frequency: 1.657632569164719e-5
allele num: 120654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.418A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+15A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+15A>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-17102531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102531
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102531
    reference: chr 8
allele count: 4
allele frequency: 3.314221323699997e-5
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+14C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.417C>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+14C>T
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11814
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27384
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

8-17102535-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102535
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102535
    reference: chr 8
allele count: 1
allele frequency: 8.278145695364238e-6
allele num: 120800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.413C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.117+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.117+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.17+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.117+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.117+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.117+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.56+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.117+10C>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.262+10C>G
  variant of: http://identifiers.org/hgnc/14101
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

8-17102553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102553
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102553
    reference: chr 8
allele count: 4
allele frequency: 3.301419610432486e-5
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.109G>A
  hgvsp: ENSP00000428783.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.109G>A
  hgvsp: ENSP00000429632.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.109G>A
  hgvsp: ENSP00000430160.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.109G>A
  hgvsp: ENSP00000355279.4:p.Val37Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.109G>A
  hgvsp: ENSP00000429093.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.109G>A
  hgvsp: ENSP00000429079.1:p.Val37Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.48G>A
  hgvsp: ENSP00000428147.1:p.Val17Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.9G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.254G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.395G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val37Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-17102561-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102561
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102561
    reference: chr 8
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.387A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.101A>G
  hgvsp: ENSP00000429632.1:p.Tyr34Cys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.101A>G
  hgvsp: ENSP00000355279.4:p.Tyr34Cys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.101A>G
  hgvsp: ENSP00000429079.1:p.Tyr34Cys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000519998
  gene symbol: CNOT7
  hgvsc: ENST00000519998.1:n.1A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.101A>G
  hgvsp: ENSP00000428783.1:p.Tyr34Cys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.246A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.40A>G
  hgvsp: ENSP00000428147.1:p.Tyr14Cys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.101A>G
  hgvsp: ENSP00000430160.1:p.Tyr34Cys
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.101A>G
  hgvsp: ENSP00000429093.1:p.Tyr34Cys
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr34Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-17102567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102567
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102567
    reference: chr 8
allele count: 2
allele frequency: 1.649484536082474e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.95G>A
  hgvsp: ENSP00000355279.4:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.95G>A
  hgvsp: ENSP00000429079.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.95G>A
  hgvsp: ENSP00000429632.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.95G>A
  hgvsp: ENSP00000429093.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.95G>A
  hgvsp: ENSP00000428783.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.34G>A
  hgvsp: ENSP00000428147.1:p.Arg12Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.95G>A
  hgvsp: ENSP00000430160.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.381G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.240G>A
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg32Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ

8-17102579-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102579
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102579
    reference: chr 8
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.83G>A
  hgvsp: ENSP00000355279.4:p.Arg28His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.369G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.22G>A
  hgvsp: ENSP00000428147.1:p.Arg8His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.83G>A
  hgvsp: ENSP00000428783.1:p.Arg28His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.83G>A
  hgvsp: ENSP00000429632.1:p.Arg28His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.228G>A
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.83G>A
  hgvsp: ENSP00000429093.1:p.Arg28His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.83G>A
  hgvsp: ENSP00000429079.1:p.Arg28His
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.83G>A
  hgvsp: ENSP00000430160.1:p.Arg28His
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg28His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/8-17102590-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102590
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102590
    reference: chr 8
allele count: 18
allele frequency: 1.484266772214526e-4
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.72G>T
  hgvsp: ENSP00000429632.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.72G>T
  hgvsp: ENSP00000429079.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.72G>T
  hgvsp: ENSP00000428783.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.217G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.11G>T
  hgvsp: ENSP00000428147.1:p.Met4Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.72G>T
  hgvsp: ENSP00000429093.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.358G>T
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.72G>T
  hgvsp: ENSP00000355279.4:p.Met24Ile
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.72G>T
  hgvsp: ENSP00000430160.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41422
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met24Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-17102592-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17102592
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17102592
    reference: chr 8
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429079
  ensembl transcript: ENST00000520178
  gene symbol: CNOT7
  hgvsc: ENST00000520178.1:c.70A>G
  hgvsp: ENSP00000429079.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428783
  ensembl transcript: ENST00000518021
  gene symbol: CNOT7
  hgvsc: ENST00000518021.1:c.70A>G
  hgvsp: ENSP00000428783.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000430160
  ensembl transcript: ENST00000524358
  gene symbol: CNOT7
  hgvsc: ENST00000524358.1:c.70A>G
  hgvsp: ENSP00000430160.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000428147
  ensembl transcript: ENST00000519918
  gene symbol: CNOT7
  hgvsc: ENST00000519918.1:c.9A>G
  hgvsp: ENSP00000428147.1:p.Met4Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000523649
  gene symbol: CNOT7
  hgvsc: ENST00000523649.1:n.356A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198791
  ensembl transcript: ENST00000518885
  gene symbol: CNOT7
  hgvsc: ENST00000518885.1:n.215A>G
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000355279
  ensembl transcript: ENST00000361272
  gene symbol: CNOT7
  hgvsc: ENST00000361272.4:c.70A>G
  hgvsp: ENSP00000355279.4:p.Met24Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429632
  ensembl transcript: ENST00000519954
  gene symbol: CNOT7
  hgvsc: ENST00000519954.1:c.70A>G
  hgvsp: ENSP00000429632.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/14101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198791
  ensembl protein: ENSP00000429093
  ensembl transcript: ENST00000523917
  gene symbol: CNOT7
  hgvsc: ENST00000523917.1:c.70A>G
  hgvsp: ENSP00000429093.1:p.Met24Val
  variant of: http://identifiers.org/hgnc/14101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met24Val
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1949
bin: 1.75e1
variant carriers: 427

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 223

GenotypeQuality
all individuals: 2382
bin: 3.75e1
variant carriers: 792

GenotypeQuality
all individuals: 1931
bin: 5.75e1
variant carriers: 672

GenotypeQuality
all individuals: 1459
bin: 6.75e1
variant carriers: 377

GenotypeQuality
all individuals: 868
bin: 9.25e1
variant carriers: 177

GenotypeQuality
all individuals: 2395
bin: 2.25e1
variant carriers: 536

GenotypeQuality
all individuals: 7051
bin: 9.75e1
variant carriers: 1039

European (Non-Finnish)
type: Population
allele count: 5346
allele frequency: 1.868708053691275e-1
allele num: 28608
num of homozygotes: 0

African
type: Population
allele count: 535
allele frequency: 1.132035548032163e-1
allele num: 4726
num of homozygotes: 0

Latino
type: Population
allele count: 526
allele frequency: 8.544509421702404e-2
allele num: 6156
num of homozygotes: 0

South Asian
type: Population
allele count: 1169
allele frequency: 1.184877356578147e-1
allele num: 9866
num of homozygotes: 0

Other
type: Population
allele count: 78
allele frequency: 1.566265060240964e-1
allele num: 498
num of homozygotes: 0

East Asian
type: Population
allele count: 184
allele frequency: 4.427333974975938e-2
allele num: 4156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 504
allele frequency: 1.392265193370166e-1
allele num: 3620
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.171e-1

DP
type: SiteQuality
SIO_000300: 1.025781e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 5.746e1

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 4.78e0

GenotypeQuality
all individuals: 1397
bin: 7.25e1
variant carriers: 71

GenotypeQuality
all individuals: 1670
bin: 6.25e1
variant carriers: 90

GenotypeQuality
all individuals: 868
bin: 9.25e1
variant carriers: 31

GenotypeQuality
all individuals: 2598
bin: 7.5e0
variant carriers: 260

GenotypeQuality
all individuals: 2114
bin: 4.75e1
variant carriers: 121

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 66

GenotypeQuality
all individuals: 1459
bin: 6.75e1
variant carriers: 79

GenotypeQuality
all individuals: 2395
bin: 2.25e1
variant carriers: 125

Other
type: Population
allele count: 4
allele frequency: 8.032128514056224e-3
allele num: 498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 295
allele frequency: 1.031180089485459e-2
allele num: 28608
num of homozygotes: 0

Latino
type: Population
allele count: 242
allele frequency: 3.931124106562703e-2
allele num: 6156
num of homozygotes: 0

African
type: Population
allele count: 121
allele frequency: 2.560304697418536e-2
allele num: 4726
num of homozygotes: 0

South Asian
type: Population
allele count: 246
allele frequency: 2.493411717007906e-2
allele num: 9866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 43
allele frequency: 1.187845303867403e-2
allele num: 3620
num of homozygotes: 0

East Asian
type: Population
allele count: 228
allele frequency: 5.48604427333975e-2
allele num: 4156
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

MQ
type: SiteQuality
SIO_000300: 5.746e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

QD
type: SiteQuality
SIO_000300: 4.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.171e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

DP
type: SiteQuality
SIO_000300: 1.025781e6

GenotypeQuality
all individuals: 2233
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 868
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1459
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2079
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1397
bin: 7.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.76243093922652e-4
allele num: 3620
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.231908590774439e-4
allele num: 4726
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 6.291946308724832e-4
allele num: 28608
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.684311838306063e-3
allele num: 4156
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 9.122237989053314e-4
allele num: 9866
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 1.624431448992852e-3
allele num: 6156
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.171e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.78e0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

DP
type: SiteQuality
SIO_000300: 1.025781e6

MQ
type: SiteQuality
SIO_000300: 5.746e1

GenotypeQuality
all individuals: 1397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 929
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 868
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1360
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.495525727069351e-5
allele num: 28608
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.812319538017325e-4
allele num: 4156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 5.746e1

DP
type: SiteQuality
SIO_000300: 1.025781e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.171e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.78e0

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

GenotypeQuality
all individuals: 2382
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2114
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 929
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 7051
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1459
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1360
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1397
bin: 7.25e1
variant carriers: 4

Latino
type: Population
allele count: 7
allele frequency: 1.137102014294997e-3
allele num: 6156
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 7.218479307025986e-4
allele num: 4156
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 2.327549724925942e-3
allele num: 4726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 1.657458563535912e-3
allele num: 3620
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 1.317656598418812e-3
allele num: 9866
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 1.004016064257028e-2
allele num: 498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 102
allele frequency: 3.565436241610738e-3
allele num: 28608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.171e-1

QD
type: SiteQuality
SIO_000300: 4.78e0

MQ
type: SiteQuality
SIO_000300: 5.746e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.025781e6

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

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.940491591203105e-3
allele num: 1546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.407e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.68e0

FS
type: SiteQuality
SIO_000300: 1.534e0

DP
type: SiteQuality
SIO_000300: 8.21897e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.832e-1

MQ
type: SiteQuality
SIO_000300: 5.777e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 4.1e0

GenotypeQuality
all individuals: 548
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2911
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3524
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.641310089804543e-4
allele num: 3786
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.289828e6

VQSLOD
type: SiteQuality
SIO_000300: 4.58e0

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.398e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.027e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.377e1

QD
type: SiteQuality
SIO_000300: 7.08e0

GenotypeQuality
all individuals: 1933
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4838
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.94114449879649e-5
allele num: 51516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

QD
type: SiteQuality
SIO_000300: 6.16e0

DP
type: SiteQuality
SIO_000300: 1.337156e6

VQSLOD
type: SiteQuality
SIO_000300: -2.307e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 5.721e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.381e0

GenotypeQuality
all individuals: 686
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 432
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6889
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.236705416769726e-4
allele num: 8086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.250869607620038e-5
allele num: 61522
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.183527083848628e-5
allele num: 16172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.455e1

DP
type: SiteQuality
SIO_000300: 1.496767e6

MQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 1.277e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.575e0

QD
type: SiteQuality
SIO_000300: 1.141e1

GenotypeQuality
all individuals: 731
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1619
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9016
num of homozygotes: 0

East Asian
type: Population
allele count: 22
allele frequency: 2.67314702308627e-3
allele num: 8230
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.159911297277319e-5
allele num: 16234
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.541363e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.305e1

VQSLOD
type: SiteQuality
SIO_000300: -1.259e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeQuality
all individuals: 509
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63938
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.572e0

QD
type: SiteQuality
SIO_000300: 1.539e1

DP
type: SiteQuality
SIO_000300: 1.606253e6

MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

FS
type: SiteQuality
SIO_000300: 8.656000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.293e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.143e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.522e0

GenotypeQuality
all individuals: 214
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.154982458299993e-5
allele num: 64988
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 5.187e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.385999999999999e0

QD
type: SiteQuality
SIO_000300: 1.187e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.618e0

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

DP
type: SiteQuality
SIO_000300: 1.634496e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 888
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.562460078474313e-5
allele num: 65754
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.677e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 7.28e0

MQ
type: SiteQuality
SIO_000300: 4.683e1

VQSLOD
type: SiteQuality
SIO_000300: -2.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

DP
type: SiteQuality
SIO_000300: 1.653234e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.92e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3015
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66024
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.657778e6

VQSLOD
type: SiteQuality
SIO_000300: -1.402e0

MQ
type: SiteQuality
SIO_000300: 4.868e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 2.623e0

QD
type: SiteQuality
SIO_000300: 1.665e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-1

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

GenotypeQuality
all individuals: 1843
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 828
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.971220185294697e-4
allele num: 10146
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66448
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.174e0

FS
type: SiteQuality
SIO_000300: 9.098000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.162e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-1

DP
type: SiteQuality
SIO_000300: 1.667983e6

QD
type: SiteQuality
SIO_000300: 1.103e1

MQRankSum
type: SiteQuality
SIO_000300: 9.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.074e0

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

GenotypeQuality
all individuals: 828
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1843
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variant carriers: 0

GenotypeQuality
all individuals: 831
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variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.668435e6

MQRankSum
type: SiteQuality
SIO_000300: 2.04e0

VQSLOD
type: SiteQuality
SIO_000300: -1.649e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

FS
type: SiteQuality
SIO_000300: 7.787e0

MQ
type: SiteQuality
SIO_000300: 5.301e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

QD
type: SiteQuality
SIO_000300: 1.552e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

GenotypeQuality
all individuals: 3019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 828
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 39311
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66478
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.061e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 3.468e0

MQRankSum
type: SiteQuality
SIO_000300: 9.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 4.782e1

DP
type: SiteQuality
SIO_000300: 1.668667e6

GenotypeQuality
all individuals: 25
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 8
allele frequency: 9.246417013407304e-4
allele num: 8652
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.182e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.037e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 1.669282e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

VQSLOD
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.539e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

DP
type: SiteQuality
SIO_000300: 1.669312e6

MQ
type: SiteQuality
SIO_000300: 4.885e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.798157946306095e-5
allele num: 10206
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.669893e6

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.737e1

ReadPosRankSum
type: SiteQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 2733
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

Latino
type: Population
allele count: 0
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

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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SIO_000300: 5.4e1

VQSLOD
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BaseQRankSum
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DP
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

South Asian
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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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South Asian
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
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DP
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10292
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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FS
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SIO_000300: 5.106e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.61e-1

DP
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BaseQRankSum
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SIO_000300: -3.659e0

VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 4.995e1

QD
type: SiteQuality
SIO_000300: 1.484e1

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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bin: 7.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66666
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.672498e6

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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variant carriers: 0

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

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

East Asian
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allele count: 1
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allele num: 8654
num of homozygotes: 0

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

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

South Asian
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African
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allele num: 10314
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VQSLOD
type: SiteQuality
SIO_000300: -7.06e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.498e1

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998320940273447e-5
allele num: 66704
num of homozygotes: 0

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

South Asian
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African
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East Asian
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allele frequency: 2.31107002542177e-4
allele num: 8654
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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DP
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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African
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Other
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South Asian
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allele num: 16506
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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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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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Other
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Latino
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African
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South Asian
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European (Non-Finnish)
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.63879e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.38e1

GenotypeQuality
all individuals: 91
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 827
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65896
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.908838684106223e-5
allele num: 10092
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

QD
type: SiteQuality
SIO_000300: 1.179e1

MQRankSum
type: SiteQuality
SIO_000300: -1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.556e0

FS
type: SiteQuality
SIO_000300: 1.161e0

DP
type: SiteQuality
SIO_000300: 1.615177e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

MQ
type: SiteQuality
SIO_000300: 5.753e1

GenotypeQuality
all individuals: 827
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8290
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 825
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14654
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.928514694201747e-5
allele num: 10072
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: 8624
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.91e-1

QD
type: SiteQuality
SIO_000300: 1.825e1

VQSLOD
type: SiteQuality
SIO_000300: -7.613e-1

FS
type: SiteQuality
SIO_000300: 1.325e0

MQ
type: SiteQuality
SIO_000300: 5.799e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 1.606065e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

GenotypeQuality
all individuals: 556
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2968
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5220700152207e-5
allele num: 65700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.214e1

VQSLOD
type: SiteQuality
SIO_000300: -1.733e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

MQ
type: SiteQuality
SIO_000300: 5.824e1

DP
type: SiteQuality
SIO_000300: 1.598199e6

FS
type: SiteQuality
SIO_000300: 2.582e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

GenotypeQuality
all individuals: 2647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 826
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variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65612
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.020499859590003e-5
allele num: 14244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.68e-1

MQ
type: SiteQuality
SIO_000300: 5.807e1

VQSLOD
type: SiteQuality
SIO_000300: -2.193e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 5.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

DP
type: SiteQuality
SIO_000300: 1.591489e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 278
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 825
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14162
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.599653379549393e-4
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.524994662518681e-4
allele num: 65574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.004e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.584e1

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.588858e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

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

GenotypeQuality
all individuals: 34538
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variant carriers: 0

GenotypeQuality
all individuals: 826
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variant carriers: 0

GenotypeQuality
all individuals: 701
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 637
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 8189
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variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14106
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.91e0

QD
type: SiteQuality
SIO_000300: 6.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.427e0

VQSLOD
type: SiteQuality
SIO_000300: -2.305e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

MQ
type: SiteQuality
SIO_000300: 5.837e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.47e0

DP
type: SiteQuality
SIO_000300: 1.586238e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.485130111524163e-4
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13786
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.588418830870882e-5
allele num: 65382
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.578222e6

MQ
type: SiteQuality
SIO_000300: 5.783e1

MQRankSum
type: SiteQuality
SIO_000300: 4.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.453e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.984e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.3e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 463
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variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 2.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65324
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.007658202337767e-4
allele num: 9924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13604
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.717e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.801e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

VQSLOD
type: SiteQuality
SIO_000300: -1.785e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.259e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

FS
type: SiteQuality
SIO_000300: 7.227e0

DP
type: SiteQuality
SIO_000300: 1.574382e6

GenotypeQuality
all individuals: 805
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 539
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GenotypeQuality
all individuals: 2903
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variant carriers: 1

GenotypeQuality
all individuals: 2631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8077
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65238
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.570671e6

QD
type: SiteQuality
SIO_000300: 1.167e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.54e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 3.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

GenotypeQuality
all individuals: 32186
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variant carriers: 0

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

Other
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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

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

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

Latino
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allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

East Asian
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FS
type: SiteQuality
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QD
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InbreedingCoeff
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65164
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South Asian
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allele frequency: 7.57002271006813e-5
allele num: 13210
num of homozygotes: 0

African
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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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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

East Asian
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allele num: 8600
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11512
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65106
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9874
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MQ
type: SiteQuality
SIO_000300: 5.763e1

QD
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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SIO_000300: 1.42e0

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

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

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

Latino
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allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

QD
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SIO_000300: 1.299e1

BaseQRankSum
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InbreedingCoeff
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DP
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VQSLOD
type: SiteQuality
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MQRankSum
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MQ
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SIO_000300: 5.909e1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -4.12e-1

ReadPosRankSum
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SIO_000300: 6.67e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 838
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: 64660
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 1.02880658436214e-4
allele num: 9720
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 2.93e0

VQSLOD
type: SiteQuality
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DP
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ClippingRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.33e-1

FS
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MQ
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SIO_000300: 5.979e1

InbreedingCoeff
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SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.854e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 836
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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 4
allele frequency: 6.206361520558573e-5
allele num: 64450
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Latino
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African
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allele frequency: 0.0e0
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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QD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.864e1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64434
num of homozygotes: 0

African
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East Asian
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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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South Asian
type: Population
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allele frequency: 8.326394671107411e-5
allele num: 12010
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Other
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

South Asian
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allele frequency: 7.198080511863503e-3
allele num: 7502
num of homozygotes: 1

Latino
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East Asian
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African
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Other
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allele num: 120
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European (Non-Finnish)
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allele frequency: 1.923076923076923e-2
allele num: 2860
num of homozygotes: 0

European (Finnish)
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allele frequency: NaN
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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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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South Asian
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allele frequency: 5.330490405117271e-4
allele num: 7504
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European (Non-Finnish)
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African
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Latino
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East Asian
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Other
type: Population
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allele frequency: 0.0e0
allele num: 120
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European (Finnish)
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allele frequency: NaN
allele num: 0
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ClippingRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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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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MQ
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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FS
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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African
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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MQRankSum
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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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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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FS
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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East Asian
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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FS
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MQ
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VQSLOD
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European (Non-Finnish)
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BaseQRankSum
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QD
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DP
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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MQRankSum
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East Asian
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European (Non-Finnish)
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African
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FS
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 2.87e0

DP
type: SiteQuality
SIO_000300: 1.823432e6

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

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 39514
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66244
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.591e0

FS
type: SiteQuality
SIO_000300: 2.815e0

QD
type: SiteQuality
SIO_000300: 1.223e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.802e0

MQ
type: SiteQuality
SIO_000300: 5.762e1

DP
type: SiteQuality
SIO_000300: 1.826736e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.887e1

FS
type: SiteQuality
SIO_000300: 4.84e0

VQSLOD
type: SiteQuality
SIO_000300: -1.018e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

DP
type: SiteQuality
SIO_000300: 1.828726e6

GenotypeQuality
all individuals: 2185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
all individuals: 457
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variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508887346470713e-5
allele num: 66274
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.015e1

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.719e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.192e0

DP
type: SiteQuality
SIO_000300: 1.831187e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 4.835e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.451e0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66300
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15982
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 1.833995e6

MQ
type: SiteQuality
SIO_000300: 5.869e1

VQSLOD
type: SiteQuality
SIO_000300: -4.32e-2

QD
type: SiteQuality
SIO_000300: 1.247e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 5.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

GenotypeQuality
all individuals: 1290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 4304
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15982
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.313208420078649e-4
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66300
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

DP
type: SiteQuality
SIO_000300: 1.833995e6

MQ
type: SiteQuality
SIO_000300: 5.869e1

FS
type: SiteQuality
SIO_000300: 5.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -4.32e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.247e1

GenotypeQuality
all individuals: 404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1885
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variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010959894014212e-5
allele num: 66424
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.418e0

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.827e1

FS
type: SiteQuality
SIO_000300: 4.357e0

QD
type: SiteQuality
SIO_000300: 1.323e1

DP
type: SiteQuality
SIO_000300: 1.842583e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.602e0

VQSLOD
type: SiteQuality
SIO_000300: -2.136e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 36
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
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: 2
allele frequency: 1.234415504258734e-4
allele num: 16202
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

QD
type: SiteQuality
SIO_000300: 1.019e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.437e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 5.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

MQ
type: SiteQuality
SIO_000300: 5.91e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.843138e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1884
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 41049
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GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.149305128520478e-5
allele num: 16262
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.845482e6

MQ
type: SiteQuality
SIO_000300: 5.716e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.404e0

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

FS
type: SiteQuality
SIO_000300: 1.6804e1

VQSLOD
type: SiteQuality
SIO_000300: -2.884e0

QD
type: SiteQuality
SIO_000300: 1.182e1

GenotypeQuality
all individuals: 1881
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4300
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 457
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8124
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 703
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003273568189326e-5
allele num: 66594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.214624073849144e-4
allele num: 16466
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.002e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.911e-1

DP
type: SiteQuality
SIO_000300: 1.852567e6

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 5.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

MQ
type: SiteQuality
SIO_000300: 5.83e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

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

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2210
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4296
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.753e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.229e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 1.853035e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.57e0

FS
type: SiteQuality
SIO_000300: 6.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
type: SiteQuality
SIO_000300: 1.645e1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4295
bin: 9.75e1
variant carriers: 2

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: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 41555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1881
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.830000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 8.432e0

QD
type: SiteQuality
SIO_000300: 1.224e1

DP
type: SiteQuality
SIO_000300: 1.85336e6

MQ
type: SiteQuality
SIO_000300: 5.813e1

GenotypeQuality
all individuals: 1290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
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variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 2206
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 4294
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 701
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 9.23e0

VQSLOD
type: SiteQuality
SIO_000300: -2.329e0

MQ
type: SiteQuality
SIO_000300: 5.048e1

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.229e0

FS
type: SiteQuality
SIO_000300: 1.024e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.97e-1

DP
type: SiteQuality
SIO_000300: 1.853213e6

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4293
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 8063
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1286
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
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variant carriers: 0

GenotypeQuality
all individuals: 701
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variant carriers: 0

GenotypeQuality
all individuals: 2193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 18
allele frequency: 2.079963022879593e-3
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.605e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.123e0

QD
type: SiteQuality
SIO_000300: 1.159e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.37e-2

DP
type: SiteQuality
SIO_000300: 1.852374e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

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

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8065
bin: 6.75e1
variant carriers: 0