2-152527565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527565
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527565
    reference: chr 2
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4478C>T
  hgvsp: ENSP00000474498.1:p.Ala1493Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4478C>T
  hgvsp: ENSP00000386259.1:p.Ala1493Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4478C>T
  hgvsp: ENSP00000380505.3:p.Ala1493Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4478C>T
  hgvsp: ENSP00000172853.10:p.Ala1493Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4478C>T
  hgvsp: ENSP00000473894.1:p.Ala1493Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4478C>T
  hgvsp: ENSP00000416578.2:p.Ala1493Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.330C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3673
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala1493Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

2-152527566-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527566
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527566
    reference: chr 2
allele count: 2
allele frequency: 1.656863557286057e-5
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4477G>C
  hgvsp: ENSP00000473894.1:p.Ala1493Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4477G>C
  hgvsp: ENSP00000474498.1:p.Ala1493Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4477G>C
  hgvsp: ENSP00000416578.2:p.Ala1493Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4477G>C
  hgvsp: ENSP00000172853.10:p.Ala1493Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4477G>C
  hgvsp: ENSP00000380505.3:p.Ala1493Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4477G>C
  hgvsp: ENSP00000386259.1:p.Ala1493Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.329G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7610
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala1493Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

2-152527572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527572
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527572
    reference: chr 2
allele count: 89152
allele frequency: 7.38563499295833e-1
allele num: 120710
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4471G>A
  hgvsp: ENSP00000172853.10:p.Val1491Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4471G>A
  hgvsp: ENSP00000380505.3:p.Val1491Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4471G>A
  hgvsp: ENSP00000473894.1:p.Val1491Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.323G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4471G>A
  hgvsp: ENSP00000416578.2:p.Val1491Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4471G>A
  hgvsp: ENSP00000386259.1:p.Val1491Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4471G>A
  hgvsp: ENSP00000474498.1:p.Val1491Met
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 7.25e1
  variant carriers: 4119
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 2.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 8.75e1
  variant carriers: 2706
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 5.25e1
  variant carriers: 3031
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 4.75e1
  variant carriers: 2282
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 589
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 5.75e1
  variant carriers: 3693
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 8.25e1
  variant carriers: 3210
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 1040
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 6.25e1
  variant carriers: 4103
genotype depth: GenotypeDepth
  all individuals: 17404
  bin: 9.75e1
  variant carriers: 17082
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 6.75e1
  variant carriers: 4341
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.75e1
  variant carriers: 298
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 9.25e1
  variant carriers: 2104
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 4.25e1
  variant carriers: 1595
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 7.75e1
  variant carriers: 3848
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 55143
  bin: 9.75e1
  variant carriers: 53667
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 8
hgvs: p.Val1491Met
num of homozygotes: 34995
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

2-152527574-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527574
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527574
    reference: chr 2
allele count: 4
allele frequency: 3.312355084465055e-5
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.321T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4469T>C
  hgvsp: ENSP00000172853.10:p.Met1490Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4469T>C
  hgvsp: ENSP00000473894.1:p.Met1490Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4469T>C
  hgvsp: ENSP00000386259.1:p.Met1490Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4469T>C
  hgvsp: ENSP00000416578.2:p.Met1490Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4469T>C
  hgvsp: ENSP00000380505.3:p.Met1490Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4469T>C
  hgvsp: ENSP00000474498.1:p.Met1490Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met1490Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

2-152527577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527577
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527577
    reference: chr 2
allele count: 58
allele frequency: 4.803073967339097e-4
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4466G>A
  hgvsp: ENSP00000416578.2:p.Gly1489Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4466G>A
  hgvsp: ENSP00000474498.1:p.Gly1489Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.318G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4466G>A
  hgvsp: ENSP00000473894.1:p.Gly1489Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4466G>A
  hgvsp: ENSP00000380505.3:p.Gly1489Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4466G>A
  hgvsp: ENSP00000172853.10:p.Gly1489Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4466G>A
  hgvsp: ENSP00000386259.1:p.Gly1489Asp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8439
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5946
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly1489Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

2-152527580-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527580
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527580
    reference: chr 2
allele count: 53
allele frequency: 4.388797800632649e-4
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4463T>C
  hgvsp: ENSP00000473894.1:p.Met1488Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4463T>C
  hgvsp: ENSP00000386259.1:p.Met1488Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4463T>C
  hgvsp: ENSP00000380505.3:p.Met1488Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.315T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4463T>C
  hgvsp: ENSP00000416578.2:p.Met1488Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4463T>C
  hgvsp: ENSP00000474498.1:p.Met1488Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4463T>C
  hgvsp: ENSP00000172853.10:p.Met1488Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met1488Thr
num of homozygotes: 1
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-152527582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527582
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527582
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4461C>T
  hgvsp: ENST00000427231.2:c.4461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4461C>T
  hgvsp: ENST00000603639.1:c.4461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.313C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4461C>T
  hgvsp: ENST00000604864.1:c.4461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4461C>T
  hgvsp: ENST00000172853.10:c.4461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4461C>T
  hgvsp: ENST00000409198.1:c.4461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4461C>T
  hgvsp: ENST00000397345.3:c.4461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5966
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser1487Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

2-152527587-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527587
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527587
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4456G>C
  hgvsp: ENSP00000380505.3:p.Asp1486His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4456G>C
  hgvsp: ENSP00000386259.1:p.Asp1486His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4456G>C
  hgvsp: ENSP00000172853.10:p.Asp1486His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4456G>C
  hgvsp: ENSP00000416578.2:p.Asp1486His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4456G>C
  hgvsp: ENSP00000474498.1:p.Asp1486His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.308G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4456G>C
  hgvsp: ENSP00000473894.1:p.Asp1486His
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5975
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp1486His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

2-152527600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527600
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527600
    reference: chr 2
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4443C>T
  hgvsp: ENST00000603639.1:c.4443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4443C>T
  hgvsp: ENST00000397345.3:c.4443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4443C>T
  hgvsp: ENST00000604864.1:c.4443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4443C>T
  hgvsp: ENST00000409198.1:c.4443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.295C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4443C>T
  hgvsp: ENST00000427231.2:c.4443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4443C>T
  hgvsp: ENST00000172853.10:c.4443C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17293
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe1481Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-152527604-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527604
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527604
    reference: chr 2
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4439A>G
  hgvsp: ENSP00000380505.3:p.Lys1480Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4439A>G
  hgvsp: ENSP00000473894.1:p.Lys1480Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4439A>G
  hgvsp: ENSP00000474498.1:p.Lys1480Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4439A>G
  hgvsp: ENSP00000386259.1:p.Lys1480Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4439A>G
  hgvsp: ENSP00000416578.2:p.Lys1480Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.291A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4439A>G
  hgvsp: ENSP00000172853.10:p.Lys1480Arg
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5945
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17299
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys1480Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-152527606-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527606
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527606
    reference: chr 2
allele count: 2
allele frequency: 1.656259834042764e-5
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4437C>G
  hgvsp: ENST00000409198.1:c.4437C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4437C>G
  hgvsp: ENST00000604864.1:c.4437C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.289C>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4437C>G
  hgvsp: ENST00000397345.3:c.4437C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4437C>G
  hgvsp: ENST00000427231.2:c.4437C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4437C>G
  hgvsp: ENST00000172853.10:c.4437C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4437C>G
  hgvsp: ENST00000603639.1:c.4437C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1824
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1479Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

2-152527608-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527608
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527608
    reference: chr 2
allele count: 22922
allele frequency: 1.898553845644143e-1
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4435G>A
  hgvsp: ENSP00000380505.3:p.Val1479Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4435G>A
  hgvsp: ENSP00000416578.2:p.Val1479Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4435G>A
  hgvsp: ENSP00000474498.1:p.Val1479Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4435G>A
  hgvsp: ENSP00000172853.10:p.Val1479Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4435G>A
  hgvsp: ENSP00000473894.1:p.Val1479Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4435G>A
  hgvsp: ENSP00000386259.1:p.Val1479Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.287G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 6.25e1
  variant carriers: 1396
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 2.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 3.75e1
  variant carriers: 491
genotype depth: GenotypeDepth
  all individuals: 21997
  bin: 2.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.25e1
  variant carriers: 664
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 1336
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 9.25e1
  variant carriers: 747
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 7.25e1
  variant carriers: 1324
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 9.75e1
  variant carriers: 6661
genotype depth: GenotypeDepth
  all individuals: 7575
  bin: 3.25e1
  variant carriers: 302
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 7.75e1
  variant carriers: 1198
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 8.75e1
  variant carriers: 900
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 5.25e1
  variant carriers: 1055
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 8.25e1
  variant carriers: 1009
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 919
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 6.75e1
  variant carriers: 1443
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 21909
  bin: 9.75e1
  variant carriers: 19528
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 2
hgvs: p.Val1479Ile
num of homozygotes: 3255
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

2-152527609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527609
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527609
    reference: chr 2
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4434C>T
  hgvsp: ENST00000603639.1:c.4434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4434C>T
  hgvsp: ENST00000427231.2:c.4434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4434C>T
  hgvsp: ENST00000604864.1:c.4434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4434C>T
  hgvsp: ENST00000397345.3:c.4434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4434C>T
  hgvsp: ENST00000409198.1:c.4434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.286C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4434C>T
  hgvsp: ENST00000172853.10:c.4434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr1478Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-152527612-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527612
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527612
    reference: chr 2
allele count: 4
allele frequency: 3.312684268062411e-5
allele num: 120748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4431T>C
  hgvsp: ENST00000604864.1:c.4431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.283T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4431T>C
  hgvsp: ENST00000409198.1:c.4431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4431T>C
  hgvsp: ENST00000427231.2:c.4431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4431T>C
  hgvsp: ENST00000397345.3:c.4431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4431T>C
  hgvsp: ENST00000603639.1:c.4431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4431T>C
  hgvsp: ENST00000172853.10:c.4431T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5351
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp1477Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

2-152527618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527618
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527618
    reference: chr 2
allele count: 6
allele frequency: 4.969108707534825e-5
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4425C>T
  hgvsp: ENST00000604864.1:c.4425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4425C>T
  hgvsp: ENST00000427231.2:c.4425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4425C>T
  hgvsp: ENST00000409198.1:c.4425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4425C>T
  hgvsp: ENST00000397345.3:c.4425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4425C>T
  hgvsp: ENST00000172853.10:c.4425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.277C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4425C>T
  hgvsp: ENST00000603639.1:c.4425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31076
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41841
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His1475His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

2-152527629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527629
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527629
    reference: chr 2
allele count: 8
allele frequency: 6.626027034190299e-5
allele num: 120736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4414T>C
  hgvsp: ENSP00000172853.10:p.Tyr1472His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4414T>C
  hgvsp: ENSP00000416578.2:p.Tyr1472His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4414T>C
  hgvsp: ENSP00000386259.1:p.Tyr1472His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4414T>C
  hgvsp: ENSP00000380505.3:p.Tyr1472His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4414T>C
  hgvsp: ENSP00000474498.1:p.Tyr1472His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4414T>C
  hgvsp: ENSP00000473894.1:p.Tyr1472His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.266T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10538
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5332
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr1472His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/2-152527630-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527630
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527630
    reference: chr 2
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4413G>T
  hgvsp: ENSP00000416578.2:p.Lys1471Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.265G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4413G>T
  hgvsp: ENSP00000474498.1:p.Lys1471Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4413G>T
  hgvsp: ENSP00000380505.3:p.Lys1471Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4413G>T
  hgvsp: ENSP00000473894.1:p.Lys1471Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4413G>T
  hgvsp: ENSP00000386259.1:p.Lys1471Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4413G>T
  hgvsp: ENSP00000172853.10:p.Lys1471Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys1471Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

2-152527631-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527631
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527631
    reference: chr 2
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4412A>C
  hgvsp: ENSP00000416578.2:p.Lys1471Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4412A>C
  hgvsp: ENSP00000386259.1:p.Lys1471Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.264A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4412A>C
  hgvsp: ENSP00000473894.1:p.Lys1471Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4412A>C
  hgvsp: ENSP00000474498.1:p.Lys1471Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4412A>C
  hgvsp: ENSP00000172853.10:p.Lys1471Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4412A>C
  hgvsp: ENSP00000380505.3:p.Lys1471Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5322
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys1471Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-152527636-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527636
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527636
    reference: chr 2
allele count: 2426
allele frequency: 2.00960901259112e-2
allele num: 120720
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.259G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4407G>C
  hgvsp: ENSP00000416578.2:p.Glu1469Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4407G>C
  hgvsp: ENSP00000386259.1:p.Glu1469Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4407G>C
  hgvsp: ENSP00000380505.3:p.Glu1469Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4407G>C
  hgvsp: ENSP00000172853.10:p.Glu1469Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4407G>C
  hgvsp: ENSP00000474498.1:p.Glu1469Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4407G>C
  hgvsp: ENSP00000473894.1:p.Glu1469Asp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31160
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 3.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 10792
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 5.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 9.75e1
  variant carriers: 704
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.75e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 216
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.75e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42042
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu1469Asp
num of homozygotes: 37
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

2-152527645-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527645
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527645
    reference: chr 2
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4398A>T
  hgvsp: ENST00000427231.2:c.4398A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4398A>T
  hgvsp: ENST00000172853.10:c.4398A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4398A>T
  hgvsp: ENST00000409198.1:c.4398A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4398A>T
  hgvsp: ENST00000604864.1:c.4398A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4398A>T
  hgvsp: ENST00000397345.3:c.4398A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4398A>T
  hgvsp: ENST00000603639.1:c.4398A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.250A>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7786
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala1466Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

2-152527645-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527645
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527645
    reference: chr 2
allele count: 7
allele frequency: 5.799983428618775e-5
allele num: 120690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4398A>G
  hgvsp: ENST00000172853.10:c.4398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.250A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4398A>G
  hgvsp: ENST00000603639.1:c.4398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4398A>G
  hgvsp: ENST00000409198.1:c.4398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4398A>G
  hgvsp: ENST00000427231.2:c.4398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4398A>G
  hgvsp: ENST00000604864.1:c.4398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4398A>G
  hgvsp: ENST00000397345.3:c.4398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32322
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7786
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala1466Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

2-152527650-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527650
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527650
    reference: chr 2
allele count: 2
allele frequency: 1.657550140891762e-5
allele num: 120660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4393G>A
  hgvsp: ENSP00000386259.1:p.Asp1465Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4393G>A
  hgvsp: ENSP00000473894.1:p.Asp1465Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4393G>A
  hgvsp: ENSP00000380505.3:p.Asp1465Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4393G>A
  hgvsp: ENSP00000172853.10:p.Asp1465Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4393G>A
  hgvsp: ENSP00000416578.2:p.Asp1465Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4393G>A
  hgvsp: ENSP00000474498.1:p.Asp1465Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.245G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7761
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp1465Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

2-152527651-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527651
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527651
    reference: chr 2
allele count: 3
allele frequency: 2.48616037391852e-5
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4392C>T
  hgvsp: ENST00000409198.1:c.4392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4392C>T
  hgvsp: ENST00000604864.1:c.4392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4392C>T
  hgvsp: ENST00000397345.3:c.4392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4392C>T
  hgvsp: ENST00000427231.2:c.4392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4392C>T
  hgvsp: ENST00000603639.1:c.4392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4392C>T
  hgvsp: ENST00000172853.10:c.4392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.244C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43789
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3398
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly1464Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

2-152527653-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527653
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527653
    reference: chr 2
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4390G>C
  hgvsp: ENSP00000380505.3:p.Gly1464Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4390G>C
  hgvsp: ENSP00000474498.1:p.Gly1464Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4390G>C
  hgvsp: ENSP00000416578.2:p.Gly1464Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.242G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4390G>C
  hgvsp: ENSP00000473894.1:p.Gly1464Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4390G>C
  hgvsp: ENSP00000386259.1:p.Gly1464Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4390G>C
  hgvsp: ENSP00000172853.10:p.Gly1464Arg
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3394
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly1464Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-152527656-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527656
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527656
    reference: chr 2
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.239G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4387G>T
  hgvsp: ENSP00000172853.10:p.Ala1463Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4387G>T
  hgvsp: ENSP00000473894.1:p.Ala1463Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4387G>T
  hgvsp: ENSP00000380505.3:p.Ala1463Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4387G>T
  hgvsp: ENSP00000416578.2:p.Ala1463Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4387G>T
  hgvsp: ENSP00000386259.1:p.Ala1463Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4387G>T
  hgvsp: ENSP00000474498.1:p.Ala1463Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43763
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3392
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala1463Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

2-152527659-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527659
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527659
    reference: chr 2
allele count: 3
allele frequency: 2.486613729423271e-5
allele num: 120646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4384A>G
  hgvsp: ENSP00000386259.1:p.Lys1462Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4384A>G
  hgvsp: ENSP00000473894.1:p.Lys1462Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4384A>G
  hgvsp: ENSP00000172853.10:p.Lys1462Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4384A>G
  hgvsp: ENSP00000474498.1:p.Lys1462Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4384A>G
  hgvsp: ENSP00000416578.2:p.Lys1462Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4384A>G
  hgvsp: ENSP00000380505.3:p.Lys1462Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.236A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3391
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys1462Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

2-152527662-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527662
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527662
    reference: chr 2
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4381A>C
  hgvsp: ENSP00000473894.1:p.Lys1461Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4381A>C
  hgvsp: ENSP00000416578.2:p.Lys1461Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4381A>C
  hgvsp: ENSP00000172853.10:p.Lys1461Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4381A>C
  hgvsp: ENSP00000474498.1:p.Lys1461Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4381A>C
  hgvsp: ENSP00000386259.1:p.Lys1461Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4381A>C
  hgvsp: ENSP00000380505.3:p.Lys1461Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.233A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43928
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys1461Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

2-152527663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527663
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527663
    reference: chr 2
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4380C>T
  hgvsp: ENST00000172853.10:c.4380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4380C>T
  hgvsp: ENST00000427231.2:c.4380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4380C>T
  hgvsp: ENST00000409198.1:c.4380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4380C>T
  hgvsp: ENST00000603639.1:c.4380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4380C>T
  hgvsp: ENST00000604864.1:c.4380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4380C>T
  hgvsp: ENST00000397345.3:c.4380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.232C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val1460Val
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

2-152527668-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527668
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527668
    reference: chr 2
allele count: 2
allele frequency: 1.658539821541115e-5
allele num: 120588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.227A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4375A>G
  hgvsp: ENSP00000380505.3:p.Lys1459Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4375A>G
  hgvsp: ENSP00000473894.1:p.Lys1459Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4375A>G
  hgvsp: ENSP00000386259.1:p.Lys1459Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4375A>G
  hgvsp: ENSP00000416578.2:p.Lys1459Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4375A>G
  hgvsp: ENSP00000172853.10:p.Lys1459Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4375A>G
  hgvsp: ENSP00000474498.1:p.Lys1459Glu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43976
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys1459Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

2-152527670-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527670
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527670
    reference: chr 2
allele count: 1
allele frequency: 8.293111741387604e-6
allele num: 120582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4373A>G
  hgvsp: ENSP00000172853.10:p.Glu1458Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4373A>G
  hgvsp: ENSP00000380505.3:p.Glu1458Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4373A>G
  hgvsp: ENSP00000416578.2:p.Glu1458Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4373A>G
  hgvsp: ENSP00000474498.1:p.Glu1458Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4373A>G
  hgvsp: ENSP00000386259.1:p.Glu1458Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4373A>G
  hgvsp: ENSP00000473894.1:p.Glu1458Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.225A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43953
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu1458Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

2-152527679-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527679
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527679
    reference: chr 2
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4364T>A
  hgvsp: ENSP00000380505.3:p.Leu1455Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.216T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4364T>A
  hgvsp: ENSP00000386259.1:p.Leu1455Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4364T>A
  hgvsp: ENSP00000416578.2:p.Leu1455Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4364T>A
  hgvsp: ENSP00000473894.1:p.Leu1455Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4364T>A
  hgvsp: ENSP00000172853.10:p.Leu1455Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4364T>A
  hgvsp: ENSP00000474498.1:p.Leu1455Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3339
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu1455Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-152527679-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527679
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527679
    reference: chr 2
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4364T>C
  hgvsp: ENSP00000473894.1:p.Leu1455Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.216T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4364T>C
  hgvsp: ENSP00000386259.1:p.Leu1455Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4364T>C
  hgvsp: ENSP00000416578.2:p.Leu1455Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4364T>C
  hgvsp: ENSP00000172853.10:p.Leu1455Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4364T>C
  hgvsp: ENSP00000474498.1:p.Leu1455Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4364T>C
  hgvsp: ENSP00000380505.3:p.Leu1455Pro
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7635
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  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: 54
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu1455Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

2-152527689-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527689
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527689
    reference: chr 2
allele count: 2
allele frequency: 1.662123529020677e-5
allele num: 120328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4354A>G
  hgvsp: ENSP00000474498.1:p.Ile1452Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4354A>G
  hgvsp: ENSP00000380505.3:p.Ile1452Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4354A>G
  hgvsp: ENSP00000416578.2:p.Ile1452Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4354A>G
  hgvsp: ENSP00000172853.10:p.Ile1452Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4354A>G
  hgvsp: ENSP00000473894.1:p.Ile1452Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4354A>G
  hgvsp: ENSP00000386259.1:p.Ile1452Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.206A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile1452Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

2-152527700-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527700
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527700
    reference: chr 2
allele count: 1
allele frequency: 8.344877079960612e-6
allele num: 119834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.195G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4343G>C
  hgvsp: ENSP00000386259.1:p.Gly1448Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4343G>C
  hgvsp: ENSP00000172853.10:p.Gly1448Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4343G>C
  hgvsp: ENSP00000473894.1:p.Gly1448Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4343G>C
  hgvsp: ENSP00000474498.1:p.Gly1448Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4343G>C
  hgvsp: ENSP00000416578.2:p.Gly1448Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4343G>C
  hgvsp: ENSP00000380505.3:p.Gly1448Ala
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43885
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly1448Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

2-152527701-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527701
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527701
    reference: chr 2
allele count: 7
allele frequency: 5.849810299008875e-5
allele num: 119662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4342G>A
  hgvsp: ENSP00000416578.2:p.Gly1448Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4342G>A
  hgvsp: ENSP00000386259.1:p.Gly1448Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.194G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4342G>A
  hgvsp: ENSP00000380505.3:p.Gly1448Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4342G>A
  hgvsp: ENSP00000474498.1:p.Gly1448Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4342G>A
  hgvsp: ENSP00000473894.1:p.Gly1448Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4342G>A
  hgvsp: ENSP00000172853.10:p.Gly1448Arg
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly1448Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

2-152527702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527702
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527702
    reference: chr 2
allele count: 5
allele frequency: 4.178435927863482e-5
allele num: 119662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4341C>T
  hgvsp: ENST00000427231.2:c.4341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4341C>T
  hgvsp: ENST00000172853.10:c.4341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4341C>T
  hgvsp: ENST00000604864.1:c.4341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.193C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4341C>T
  hgvsp: ENST00000397345.3:c.4341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4341C>T
  hgvsp: ENST00000409198.1:c.4341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4341C>T
  hgvsp: ENST00000603639.1:c.4341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31762
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10063
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7285
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43798
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile1447Ile
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

2-152527705-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527705
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527705
    reference: chr 2
allele count: 3
allele frequency: 2.512015808952824e-5
allele num: 119426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4338C>T
  hgvsp: ENST00000409198.1:c.4338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4338C>T
  hgvsp: ENST00000172853.10:c.4338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.190C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4338C>T
  hgvsp: ENST00000397345.3:c.4338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4338C>T
  hgvsp: ENST00000604864.1:c.4338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4338C>T
  hgvsp: ENST00000603639.1:c.4338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4338C>T
  hgvsp: ENST00000427231.2:c.4338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43663
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly1446Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

2-152527706-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527706
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527706
    reference: chr 2
allele count: 3
allele frequency: 2.513699663164245e-5
allele num: 119346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4337G>A
  hgvsp: ENSP00000172853.10:p.Gly1446Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4337G>A
  hgvsp: ENSP00000380505.3:p.Gly1446Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4337G>A
  hgvsp: ENSP00000386259.1:p.Gly1446Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4337G>A
  hgvsp: ENSP00000474498.1:p.Gly1446Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4337G>A
  hgvsp: ENSP00000473894.1:p.Gly1446Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4337G>A
  hgvsp: ENSP00000416578.2:p.Gly1446Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.189G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31537
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43642
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly1446Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-152527709-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527709
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527709
    reference: chr 2
allele count: 1
allele frequency: 8.41226845231085e-6
allele num: 118874
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4334A>C
  hgvsp: ENSP00000473894.1:p.Lys1445Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4334A>C
  hgvsp: ENSP00000474498.1:p.Lys1445Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4334A>C
  hgvsp: ENSP00000380505.3:p.Lys1445Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4334A>C
  hgvsp: ENSP00000172853.10:p.Lys1445Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4334A>C
  hgvsp: ENSP00000416578.2:p.Lys1445Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4334A>C
  hgvsp: ENSP00000386259.1:p.Lys1445Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.186A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7049
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys1445Thr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-152527728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527728
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527728
    reference: chr 2
allele count: 2
allele frequency: 1.775284489339416e-5
allele num: 112658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4315G>A
  hgvsp: ENSP00000172853.10:p.Glu1439Lys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4315G>A
  hgvsp: ENSP00000416578.2:p.Glu1439Lys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4315G>A
  hgvsp: ENSP00000473894.1:p.Glu1439Lys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.167G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4315G>A
  hgvsp: ENSP00000380505.3:p.Glu1439Lys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4315G>A
  hgvsp: ENSP00000386259.1:p.Glu1439Lys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4315G>A
  hgvsp: ENSP00000474498.1:p.Glu1439Lys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5541
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu1439Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

2-152527732-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527732
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527732
    reference: chr 2
allele count: 1
allele frequency: 9.053378720938654e-6
allele num: 110456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4311A>T
  hgvsp: ENSP00000386259.1:p.Lys1437Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4311A>T
  hgvsp: ENSP00000473894.1:p.Lys1437Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4311A>T
  hgvsp: ENSP00000474498.1:p.Lys1437Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.163A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4311A>T
  hgvsp: ENSP00000172853.10:p.Lys1437Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4311A>T
  hgvsp: ENSP00000416578.2:p.Lys1437Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4311A>T
  hgvsp: ENSP00000380505.3:p.Lys1437Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5037
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys1437Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

2-152527738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527738
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527738
    reference: chr 2
allele count: 5
allele frequency: 4.650211119584829e-5
allele num: 107522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.157G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4305G>A
  hgvsp: ENST00000603639.1:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4305G>A
  hgvsp: ENST00000397345.3:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4305G>A
  hgvsp: ENST00000427231.2:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4305G>A
  hgvsp: ENST00000409198.1:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4305G>A
  hgvsp: ENST00000604864.1:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4305G>A
  hgvsp: ENST00000172853.10:c.4305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13447
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3233
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Val1435Val
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-152527739-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527739
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527739
    reference: chr 2
allele count: 1
allele frequency: 9.396553344233335e-6
allele num: 106422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4304T>C
  hgvsp: ENSP00000172853.10:p.Val1435Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4304T>C
  hgvsp: ENSP00000473894.1:p.Val1435Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.156T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4304T>C
  hgvsp: ENSP00000386259.1:p.Val1435Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4304T>C
  hgvsp: ENSP00000416578.2:p.Val1435Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4304T>C
  hgvsp: ENSP00000474498.1:p.Val1435Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4304T>C
  hgvsp: ENSP00000380505.3:p.Val1435Ala
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9554
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14736
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val1435Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

2-152527743-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527743
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527743
    reference: chr 2
allele count: 1
allele frequency: 9.548362455838823e-6
allele num: 104730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300A>C
  hgvsp: ENSP00000172853.10:p.Asn1434His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300A>C
  hgvsp: ENSP00000473894.1:p.Asn1434His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300A>C
  hgvsp: ENSP00000474498.1:p.Asn1434His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300A>C
  hgvsp: ENSP00000416578.2:p.Asn1434His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300A>C
  hgvsp: ENSP00000386259.1:p.Asn1434His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300A>C
  hgvsp: ENSP00000380505.3:p.Asn1434His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.152A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16777
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn1434His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-152527747-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527747
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527747
    reference: chr 2
allele count: 2
allele frequency: 1.979022362952701e-5
allele num: 101060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.148A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16102
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3478
  bin: 6.75e1
  variant carriers: 0
hgvs: c.4300-4A>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-152527760-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527760
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527760
    reference: chr 2
allele count: 3
allele frequency: 3.212610567347026e-5
allele num: 93382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.135A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-17A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-17A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-17A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-17A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-17A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-17A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22884
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4563
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4040
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

2-152527765-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527765
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527765
    reference: chr 2
allele count: 1
allele frequency: 1.108131468717449e-5
allele num: 90242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-22A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-22A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.130A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-22A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-22A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-22A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-22A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24653
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4518
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28890
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4520
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum

2-152527765-TGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527765
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527763
    reference: chr 2
allele count: 1
allele frequency: 1.108131468717449e-5
allele num: 90242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.128_129delTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-24_4300-23delTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-24_4300-23delTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-24_4300-23delTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-24_4300-23delTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-24_4300-23delTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-24_4300-23delTC
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24653
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4518
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: TGA
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

2-152527773-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527773
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527773
    reference: chr 2
allele count: 1
allele frequency: 1.187169076619892e-5
allele num: 84234
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-30A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-30A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-30A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-30A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-30A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.122A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-30A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5172
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27490
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

2-152527784-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527784
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527784
    reference: chr 2
allele count: 1
allele frequency: 1.358732574254735e-5
allele num: 73598
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-41T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-41T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.111T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-41T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-41T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-41T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-41T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18838
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3400
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5074
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6399
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

2-152527792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527792
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527792
    reference: chr 2
allele count: 1
allele frequency: 1.497723460340283e-5
allele num: 66768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-49C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-49C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-49C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-49C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.103C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-49C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-49C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18914
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16852
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6642
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4939
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

2-152527793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152527793
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152527793
    reference: chr 2
allele count: 1
allele frequency: 1.584334104375931e-5
allele num: 63118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4300-50C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4300-50C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4300-50C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4300-50C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000484968
  gene symbol: NEB
  hgvsc: ENST00000484968.1:n.102C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4300-50C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4300-50C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21161
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4978
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6385
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 13375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

2-152528833-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528833
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528832
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 96030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+49delA
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+49delA
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+49delA
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+49delA
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+49delA
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+49delA
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8094
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6453
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2483
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: AT
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

2-152528834-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528834
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528834
    reference: chr 2
allele count: 26
allele frequency: 2.706585330307509e-4
allele num: 96062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+49A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+49A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+49A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+49A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+49A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+49A>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13260
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15697
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7521
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4983
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6449
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3866
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6625
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-152528834-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528834
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528834
    reference: chr 2
allele count: 6
allele frequency: 6.245966146863484e-5
allele num: 96062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+49A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+49A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+49A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+49A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+49A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+49A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13260
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15697
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5270
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6625
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2453
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 1276
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genotype quality: GenotypeQuality
  all individuals: 4983
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3866
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-152528837-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528837
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528837
    reference: chr 2
allele count: 2
allele frequency: 2.077706212341575e-5
allele num: 96260
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+46A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+46A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+46A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+46A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+46A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+46A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15631
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11714
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6491
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5038
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6607
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1237
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-152528841-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528841
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528841
    reference: chr 2
allele count: 2
allele frequency: 2.074344507135745e-5
allele num: 96416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+42A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+42A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+42A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+42A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+42A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+42A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15335
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4955
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 2800
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

2-152528842-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528842
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528842
    reference: chr 2
allele count: 1
allele frequency: 1.037000165920027e-5
allele num: 96432
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+41A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+41A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+41A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+41A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+41A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+41A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15204
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 3311
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-152528850-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528850
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528850
    reference: chr 2
allele count: 2
allele frequency: 2.051745009130265e-5
allele num: 97478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+33T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+33T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+33T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+33T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+33T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+33T>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 500
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-152528870-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528870
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528870
    reference: chr 2
allele count: 1
allele frequency: 9.643015563827121e-6
allele num: 103702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+13A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29403
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/2-152528872-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528872
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528872
    reference: chr 2
allele count: 1
allele frequency: 9.589382635545923e-6
allele num: 104282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+11G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+11G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+11G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+11G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+11G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+11G>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31615
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

2-152528874-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528874
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528874
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 105018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+9G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6056
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

2-152528876-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528876
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528876
    reference: chr 2
allele count: 10
allele frequency: 9.449295082586839e-5
allele num: 105828
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+7A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+7A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+7A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+7A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+7A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+7A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
hgvs: c.4299+7A>G
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

2-152528879-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528879
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528879
    reference: chr 2
allele count: 1
allele frequency: 9.362945208044642e-6
allele num: 106804
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4299+4A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4299+4A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4299+4A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4299+4A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4299+4A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4299+4A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5049
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5651
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5000
  bin: 6.75e1
  variant carriers: 0
hgvs: c.4299+4A>C
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

2-152528884-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528884
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528884
    reference: chr 2
allele count: 2
allele frequency: 1.850960648576611e-5
allele num: 108052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4298A>C
  hgvsp: ENSP00000474498.1:p.Asp1433Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4298A>C
  hgvsp: ENSP00000172853.10:p.Asp1433Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4298A>C
  hgvsp: ENSP00000473894.1:p.Asp1433Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4298A>C
  hgvsp: ENSP00000380505.3:p.Asp1433Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4298A>C
  hgvsp: ENSP00000416578.2:p.Asp1433Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4298A>C
  hgvsp: ENSP00000386259.1:p.Asp1433Ala
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Asp1433Ala
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

2-152528887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528887
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528887
    reference: chr 2
allele count: 2
allele frequency: 1.836985873578632e-5
allele num: 108874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4295G>A
  hgvsp: ENSP00000473894.1:p.Ser1432Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4295G>A
  hgvsp: ENSP00000416578.2:p.Ser1432Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4295G>A
  hgvsp: ENSP00000380505.3:p.Ser1432Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4295G>A
  hgvsp: ENSP00000474498.1:p.Ser1432Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4295G>A
  hgvsp: ENSP00000172853.10:p.Ser1432Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4295G>A
  hgvsp: ENSP00000386259.1:p.Ser1432Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5267
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5065
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser1432Asn
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-152528893-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528893
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528893
    reference: chr 2
allele count: 1
allele frequency: 9.059940566789881e-6
allele num: 110376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4289T>A
  hgvsp: ENSP00000473894.1:p.Ile1430Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4289T>A
  hgvsp: ENSP00000416578.2:p.Ile1430Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4289T>A
  hgvsp: ENSP00000380505.3:p.Ile1430Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4289T>A
  hgvsp: ENSP00000386259.1:p.Ile1430Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4289T>A
  hgvsp: ENSP00000172853.10:p.Ile1430Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4289T>A
  hgvsp: ENSP00000474498.1:p.Ile1430Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2529
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4641
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile1430Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

2-152528899-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528899
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528899
    reference: chr 2
allele count: 9
allele frequency: 8.067407673001075e-5
allele num: 111560
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4283A>G
  hgvsp: ENSP00000386259.1:p.Asn1428Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4283A>G
  hgvsp: ENSP00000172853.10:p.Asn1428Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4283A>G
  hgvsp: ENSP00000474498.1:p.Asn1428Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4283A>G
  hgvsp: ENSP00000416578.2:p.Asn1428Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4283A>G
  hgvsp: ENSP00000380505.3:p.Asn1428Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4283A>G
  hgvsp: ENSP00000473894.1:p.Asn1428Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34992
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5549
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn1428Ser
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

2-152528910-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528910
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528910
    reference: chr 2
allele count: 236
allele frequency: 2.066513721300853e-3
allele num: 114202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4272G>C
  hgvsp: ENST00000427231.2:c.4272G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4272G>C
  hgvsp: ENST00000604864.1:c.4272G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4272G>C
  hgvsp: ENST00000603639.1:c.4272G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4272G>C
  hgvsp: ENST00000397345.3:c.4272G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4272G>C
  hgvsp: ENST00000172853.10:c.4272G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4272G>C
  hgvsp: ENST00000409198.1:c.4272G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35683
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9908
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1735
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5715
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr1424Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

2-152528910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528910
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528910
    reference: chr 2
allele count: 7
allele frequency: 6.129489851316089e-5
allele num: 114202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4272G>A
  hgvsp: ENST00000172853.10:c.4272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4272G>A
  hgvsp: ENST00000397345.3:c.4272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4272G>A
  hgvsp: ENST00000604864.1:c.4272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4272G>A
  hgvsp: ENST00000427231.2:c.4272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4272G>A
  hgvsp: ENST00000603639.1:c.4272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4272G>A
  hgvsp: ENST00000409198.1:c.4272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5296
  bin: 9.75e1
  variant carriers: 7
hgvs: p.Thr1424Thr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

2-152528911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528911
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528911
    reference: chr 2
allele count: 2
allele frequency: 1.74076524039968e-5
allele num: 114892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4271C>T
  hgvsp: ENSP00000386259.1:p.Thr1424Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4271C>T
  hgvsp: ENSP00000474498.1:p.Thr1424Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4271C>T
  hgvsp: ENSP00000380505.3:p.Thr1424Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4271C>T
  hgvsp: ENSP00000473894.1:p.Thr1424Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4271C>T
  hgvsp: ENSP00000416578.2:p.Thr1424Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4271C>T
  hgvsp: ENSP00000172853.10:p.Thr1424Met
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5784
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr1424Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-152528917-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152528917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152528917
    reference: chr 2
allele count: 5
allele frequency: 4.288826748554665e-5
allele num: 116582
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.4265A>C
  hgvsp: ENSP00000473894.1:p.Glu1422Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.4265A>C
  hgvsp: ENSP00000386259.1:p.Glu1422Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.4265A>C
  hgvsp: ENSP00000172853.10:p.Glu1422Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.4265A>C
  hgvsp: ENSP00000380505.3:p.Glu1422Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.4265A>C
  hgvsp: ENSP00000416578.2:p.Glu1422Ala
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.4265A>C
  hgvsp: ENSP00000474498.1:p.Glu1422Ala
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5872
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5164
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2698
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu1422Ala
num of homozygotes: 0
reference allele: T

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

GenotypeQuality
all individuals: 63
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7609
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13568
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.2906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 2.072707e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.662e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

QD
type: SiteQuality
SIO_000300: 3.277e1

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

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5235
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13574
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3675
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2610
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.830000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.76e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

FS
type: SiteQuality
SIO_000300: 2.861e0

DP
type: SiteQuality
SIO_000300: 2.073005e6

QD
type: SiteQuality
SIO_000300: 1.488e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2242
bin: 6.25e1
variant carriers: 24

GenotypeQuality
all individuals: 394
bin: 9.25e1
variant carriers: 128

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 12

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 36

GenotypeQuality
all individuals: 737
bin: 6.75e1
variant carriers: 28

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 60

GenotypeQuality
all individuals: 569
bin: 7.75e1
variant carriers: 56

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 14

GenotypeQuality
all individuals: 536
bin: 8.25e1
variant carriers: 103

European (Finnish)
type: Population
allele count: 5747
allele frequency: 8.694402420574886e-1
allele num: 6610
num of homozygotes: 2503

African
type: Population
allele count: 2772
allele frequency: 2.823960880195599e-1
allele num: 9816
num of homozygotes: 423

Latino
type: Population
allele count: 9967
allele frequency: 8.616009681881052e-1
allele num: 11568
num of homozygotes: 4292

South Asian
type: Population
allele count: 10715
allele frequency: 6.490792343106373e-1
allele num: 16508
num of homozygotes: 3488

East Asian
type: Population
allele count: 3495
allele frequency: 4.07058001397624e-1
allele num: 8586
num of homozygotes: 701

Other
type: Population
allele count: 697
allele frequency: 7.744444444444445e-1
allele num: 900
num of homozygotes: 271

European (Non-Finnish)
type: Population
allele count: 55759
allele frequency: 8.35691376157789e-1
allele num: 66722
num of homozygotes: 23317

QD
type: SiteQuality
SIO_000300: 2.634e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.253e0

VQSLOD
type: SiteQuality
SIO_000300: 7.79e0

DP
type: SiteQuality
SIO_000300: 5.319741e6

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

GenotypeQuality
all individuals: 764
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5957
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31072
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17340
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 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: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.729e0

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

QD
type: SiteQuality
SIO_000300: 1.093e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

FS
type: SiteQuality
SIO_000300: 1.166e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.674098e6

MQ
type: SiteQuality
SIO_000300: 5.935e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17369
bin: 9.75e1
variant carriers: 57

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

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 753
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
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: 54
allele frequency: 5.50234359078867e-3
allele num: 9814
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.183e0

DP
type: SiteQuality
SIO_000300: 2.678734e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.196e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

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

GenotypeQuality
all individuals: 17363
bin: 9.75e1
variant carriers: 52

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

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

GenotypeQuality
all individuals: 752
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5947
bin: 6.75e1
variant carriers: 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: 8622
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.446725610669864e-4
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 29
allele frequency: 4.384638645297853e-3
allele num: 6614
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.680201e6

VQSLOD
type: SiteQuality
SIO_000300: 5.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

QD
type: SiteQuality
SIO_000300: 1.33e1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeQuality
all individuals: 1177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31159
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 545
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17309
bin: 9.75e1
variant carriers: 1

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

QD
type: SiteQuality
SIO_000300: 2.886e1

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 2.674747e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.937e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 546
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1190
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17295
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 9812
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -4.38e-1

QD
type: SiteQuality
SIO_000300: 1.945e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 7.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.024e0

DP
type: SiteQuality
SIO_000300: 2.672808e6

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

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

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31178
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 750
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 1.941e0

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

QD
type: SiteQuality
SIO_000300: 2.573e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

DP
type: SiteQuality
SIO_000300: 2.675157e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 1160
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31222
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 7.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.438e1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

DP
type: SiteQuality
SIO_000300: 2.676653e6

FS
type: SiteQuality
SIO_000300: 4.738e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31127
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17279
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 5960
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 9.25e1
variant carriers: 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: 66730
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.038735983690112e-4
allele num: 9810
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 1.786e0

DP
type: SiteQuality
SIO_000300: 2.672196e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.855e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.089e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 3.077e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

GenotypeQuality
all individuals: 5257
bin: 6.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1186
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 341
bin: 9.25e1
variant carriers: 32

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 627
bin: 8.25e1
variant carriers: 19

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 29490
bin: 6.25e1
variant carriers: 11

Latino
type: Population
allele count: 1212
allele frequency: 1.048261546445252e-1
allele num: 11562
num of homozygotes: 65

East Asian
type: Population
allele count: 4731
allele frequency: 5.497327445967929e-1
allele num: 8606
num of homozygotes: 1277

European (Non-Finnish)
type: Population
allele count: 7363
allele frequency: 1.103467913556934e-1
allele num: 66726
num of homozygotes: 393

European (Finnish)
type: Population
allele count: 783
allele frequency: 1.18385243423042e-1
allele num: 6614
num of homozygotes: 48

African
type: Population
allele count: 3824
allele frequency: 3.894093686354379e-1
allele num: 9820
num of homozygotes: 738

South Asian
type: Population
allele count: 4860
allele frequency: 2.94402713835716e-1
allele num: 16508
num of homozygotes: 721

Other
type: Population
allele count: 149
allele frequency: 1.65924276169265e-1
allele num: 898
num of homozygotes: 13

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 3.146067e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.136e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.38e0

QD
type: SiteQuality
SIO_000300: 1.587e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.17e-1

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

GenotypeQuality
all individuals: 1720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41994
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 370
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5360
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
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: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.363e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 7.96e-1

FS
type: SiteQuality
SIO_000300: 1.111e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

DP
type: SiteQuality
SIO_000300: 1.922531e6

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 901
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42032
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

African
type: Population
allele count: 4
allele frequency: 4.077471967380224e-4
allele num: 9810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 898
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.44e0

MQRankSum
type: SiteQuality
SIO_000300: -1.069e0

FS
type: SiteQuality
SIO_000300: 2.484e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

QD
type: SiteQuality
SIO_000300: 1.425e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.922018e6

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

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5406
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 7616
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991727610598249e-5
allele num: 66728
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: 11570
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.824e1

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.921859e6

GenotypeQuality
all individuals: 886
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42033
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.198897014746433e-4
allele num: 66728
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

DP
type: SiteQuality
SIO_000300: 1.919374e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

FS
type: SiteQuality
SIO_000300: 2.543e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.023e0

VQSLOD
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

GenotypeQuality
all individuals: 884
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 513
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5325
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1701
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42073
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7589
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.918985e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.708e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.904e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.743e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1709
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7587
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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: 11566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
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: 66728
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

FS
type: SiteQuality
SIO_000300: 3.371e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

DP
type: SiteQuality
SIO_000300: 1.918801e6

QD
type: SiteQuality
SIO_000300: 1.433e1

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

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

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5643
bin: 9.75e1
variant carriers: 2385

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7534
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1195
allele frequency: 1.791120836955544e-2
allele num: 66718
num of homozygotes: 6

Latino
type: Population
allele count: 101
allele frequency: 8.732491786270101e-3
allele num: 11566
num of homozygotes: 1

Other
type: Population
allele count: 9
allele frequency: 1.002227171492205e-2
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 32
allele frequency: 3.712296983758701e-3
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 527
allele frequency: 5.376453784941849e-2
allele num: 9802
num of homozygotes: 20

European (Finnish)
type: Population
allele count: 84
allele frequency: 1.27003326277593e-2
allele num: 6614
num of homozygotes: 1

South Asian
type: Population
allele count: 478
allele frequency: 2.896618591685856e-2
allele num: 16502
num of homozygotes: 9

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

QD
type: SiteQuality
SIO_000300: 1.378e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

DP
type: SiteQuality
SIO_000300: 1.924486e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1701
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
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: 11560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 1.780726e6

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.367e1

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

FS
type: SiteQuality
SIO_000300: 1.144e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

GenotypeQuality
all individuals: 1701
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 6
allele frequency: 6.124948958758677e-4
allele num: 9796
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 1.144e0

DP
type: SiteQuality
SIO_000300: 1.780726e6

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

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

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43708
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.043318348998774e-4
allele num: 9788
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
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: 898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.71e-1

FS
type: SiteQuality
SIO_000300: 2.428e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.559e0

DP
type: SiteQuality
SIO_000300: 1.77922e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

QD
type: SiteQuality
SIO_000300: 2.428e1

GenotypeQuality
all individuals: 1694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99868058054456e-5
allele num: 66696
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 1.364e0

MQRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.778706e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.05e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 7757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43840
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 324
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.725e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.3631e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.673e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.72e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.778079e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 320
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
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: 16488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.058e0

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.037e1

FS
type: SiteQuality
SIO_000300: 1.0928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.336e0

DP
type: SiteQuality
SIO_000300: 1.77717e6

GenotypeQuality
all individuals: 441
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43863
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 16490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498560460652591e-5
allele num: 66688
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.776428e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.519e0

QD
type: SiteQuality
SIO_000300: 1.347e1

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

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

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3386
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 316
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.776127e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e0

VQSLOD
type: SiteQuality
SIO_000300: -7.513e-1

QD
type: SiteQuality
SIO_000300: 1.038e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.2e-2

GenotypeQuality
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bin: 8.75e1
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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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.583e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.905e0

FS
type: SiteQuality
SIO_000300: 1.181e0

QD
type: SiteQuality
SIO_000300: 2.694e1

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.775838e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.706e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.774427e6

QD
type: SiteQuality
SIO_000300: 1.297e1

FS
type: SiteQuality
SIO_000300: 4.107e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.524e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.78e-1

FS
type: SiteQuality
SIO_000300: 3.705e0

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

DP
type: SiteQuality
SIO_000300: 1.77367e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.769739e6

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.094e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.0526e1

QD
type: SiteQuality
SIO_000300: 1.274e1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.02e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.274e1

VQSLOD
type: SiteQuality
SIO_000300: -8.094e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 1.0526e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.02e-1

DP
type: SiteQuality
SIO_000300: 1.769739e6

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

African
type: Population
allele count: 1
allele frequency: 1.023960679909891e-4
allele num: 9766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 1.36e0

DP
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9724
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508568670045861e-5
allele num: 66288
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.753882e6

FS
type: SiteQuality
SIO_000300: 1.527e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
type: SiteQuality
SIO_000300: 4.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.32e0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
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European (Finnish)
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allele count: 6
allele frequency: 9.090909090909091e-4
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66204
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

QD
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SIO_000300: 1.23e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 1.750566e6

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 394
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.064852274120387e-4
allele num: 16314
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66208
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.2e0

FS
type: SiteQuality
SIO_000300: 1.704e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.843657817109145e-4
allele num: 16272
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66088
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.601e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.944e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.03e-1

DP
type: SiteQuality
SIO_000300: 1.743537e6

MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.94e-2

QD
type: SiteQuality
SIO_000300: 1.008e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
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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: 3

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.22955858846674e-4
allele num: 16266
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.795074758135444e-5
allele num: 11370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66030
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

FS
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 1.741285e6

VQSLOD
type: SiteQuality
SIO_000300: -2.632e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

QD
type: SiteQuality
SIO_000300: 8.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 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: 11306
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17813383600377e-4
allele num: 8488
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65782
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

QD
type: SiteQuality
SIO_000300: 7.41e0

DP
type: SiteQuality
SIO_000300: 1.731165e6

VQSLOD
type: SiteQuality
SIO_000300: -2.083e0

FS
type: SiteQuality
SIO_000300: 6.83e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 222
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variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.205847465777578e-5
allele num: 62386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15396
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 1.31e1

FS
type: SiteQuality
SIO_000300: 4.055e0

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

DP
type: SiteQuality
SIO_000300: 1.591481e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 940
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
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variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.63414713860836e-5
allele num: 61194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.989e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

FS
type: SiteQuality
SIO_000300: 7.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
SIO_000300: 1.538027e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 1.405e1

VQSLOD
type: SiteQuality
SIO_000300: -4.66e-2

GenotypeQuality
all individuals: 1167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 842
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GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 276
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31379
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variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.586592178770949e-4
allele num: 8950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59526
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.474004e6

QD
type: SiteQuality
SIO_000300: 1.134e1

GenotypeQuality
all individuals: 4422
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 253
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9478
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.325908247149297e-4
allele num: 7542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.242e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

DP
type: SiteQuality
SIO_000300: 1.446899e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 3.132e0

VQSLOD
type: SiteQuality
SIO_000300: 4.61e-1

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 331
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.724494723046147e-5
allele num: 57988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.349e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

DP
type: SiteQuality
SIO_000300: 1.404154e6

VQSLOD
type: SiteQuality
SIO_000300: -9.976e-1

MQ
type: SiteQuality
SIO_000300: 5.664e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.321e0

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2057
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5874
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.576921701183961e-5
allele num: 55914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7094
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8742
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.023e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.313518e6

MQ
type: SiteQuality
SIO_000300: 5.875e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

QD
type: SiteQuality
SIO_000300: 1.467e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 219
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
all individuals: 3211
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 560
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GenotypeQuality
all individuals: 275
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.804953560371517e-5
allele num: 51680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5604
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.67e-1

DP
type: SiteQuality
SIO_000300: 1.113234e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

FS
type: SiteQuality
SIO_000300: 3.093e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

QD
type: SiteQuality
SIO_000300: 1.509e1

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.001441037547034e-5
allele num: 49964
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.045119e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

QD
type: SiteQuality
SIO_000300: 7.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

GenotypeQuality
all individuals: 4520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.001441037547034e-5
allele num: 49964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 7.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.045119e6

GenotypeQuality
all individuals: 1329
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5694
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.223684210526316e-5
allele num: 12160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5336
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

DP
type: SiteQuality
SIO_000300: 9.61375e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.103e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 268
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
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variant carriers: 0

GenotypeQuality
all individuals: 724
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variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5018
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.07641196013289e-4
allele num: 4816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.86445e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.761e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.735e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

GenotypeQuality
all individuals: 1336
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6006
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.712232167073501e-5
allele num: 36870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4262
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.922e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.044e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 8.69693e5

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 410
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GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.865657955066483e-5
allele num: 34896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4038
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.69131e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: -5.986e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 2.444e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

QD
type: SiteQuality
SIO_000300: 1.163e1

GenotypeQuality
all individuals: 5573
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4959
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4037
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7568
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

DP
type: SiteQuality
SIO_000300: 1.135728e6

QD
type: SiteQuality
SIO_000300: 5.95e0

GenotypeQuality
all individuals: 3288
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5853
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1276
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5270
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 25
allele frequency: 2.815949538184276e-3
allele num: 8878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.077121930202499e-4
allele num: 9284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56186
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.418e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

DP
type: SiteQuality
SIO_000300: 1.137085e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 2210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3288
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.067881678709999e-4
allele num: 56186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.418e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.137085e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7947
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6415
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4956
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 997
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.148227712137487e-4
allele num: 9310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.144398e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

QD
type: SiteQuality
SIO_000300: 1.058e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

FS
type: SiteQuality
SIO_000300: 3.203e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3822
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.548112404200965e-5
allele num: 56368
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.162438e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 1.825e1

FS
type: SiteQuality
SIO_000300: 3.68e0

MQRankSum
type: SiteQuality
SIO_000300: -6.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.766e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

GenotypeQuality
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bin: 2.25e1
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
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.311303435615001e-4
allele num: 7626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56376
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7298
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8930
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.951e-1

QD
type: SiteQuality
SIO_000300: 1.519e1

MQRankSum
type: SiteQuality
SIO_000300: -1.222e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

DP
type: SiteQuality
SIO_000300: 1.167616e6

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: 1557
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8988
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.111040743086342e-4
allele num: 9474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.511e0

DP
type: SiteQuality
SIO_000300: 1.224173e6

QD
type: SiteQuality
SIO_000300: 1.153e1

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: 4593
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variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.653821982601793e-5
allele num: 60466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e0

DP
type: SiteQuality
SIO_000300: 1.397596e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.256e0

QD
type: SiteQuality
SIO_000300: 1.66e1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

GenotypeQuality
all individuals: 5032
bin: 9.75e1
variant carriers: 1

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: 1672
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variant carriers: 0

GenotypeQuality
all individuals: 4696
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.644682740699319e-5
allele num: 60802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9320
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: -4.885e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

QD
type: SiteQuality
SIO_000300: 1.027e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.411562e6

GenotypeQuality
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bin: 2.75e1
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: 322
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variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8084
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.407e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.203e0

VQSLOD
type: SiteQuality
SIO_000300: -1.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.001e0

DP
type: SiteQuality
SIO_000300: 1.42419e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 10

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 10
allele frequency: 1.064282673478076e-3
allele num: 9396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8706
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10742
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

QD
type: SiteQuality
SIO_000300: 1.357e1

DP
type: SiteQuality
SIO_000300: 1.435015e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.61051343168202e-5
allele num: 62092
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.449643e6

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

QD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -8.93e-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
all individuals: 188
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.074410163339382e-5
allele num: 11020
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9500
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594336915276936e-5
allele num: 62722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.513e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.02e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.942e1

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
all individuals: 189
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63116
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.392344497607656e-4
allele num: 8360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.482095e6

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.253e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

BaseQRankSum
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SIO_000300: -4.454e0

MQRankSum
type: SiteQuality
SIO_000300: -4.85e-1

FS
type: SiteQuality
SIO_000300: 1.174e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.8e-1

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5433
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568578240682645e-5
allele num: 63752
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.441e0

QD
type: SiteQuality
SIO_000300: 7.99e0

VQSLOD
type: SiteQuality
SIO_000300: -8.02e-1

DP
type: SiteQuality
SIO_000300: 1.502234e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.55e-1

GenotypeQuality
all individuals: 4242
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5087
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 755
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35474
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 8
allele frequency: 7.646721468170522e-4
allele num: 10462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
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: 11362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64174
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.474e1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

DP
type: SiteQuality
SIO_000300: 1.516985e6

GenotypeQuality
all individuals: 2060
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5296
bin: 9.75e1
variant carriers: 235

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.239259517988125e-4
allele num: 11452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 182
allele frequency: 2.800344657804038e-3
allele num: 64992
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 1.99700449326011e-3
allele num: 12018
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.056766762649116e-4
allele num: 9724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 21
allele frequency: 3.179890975166566e-3
allele num: 6604
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.199040767386091e-3
allele num: 834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.555816e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 5.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

GenotypeQuality
all individuals: 226
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5715
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.231905465288036e-5
allele num: 64992
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.732099196646873e-5
allele num: 11452
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 5.77e-1

DP
type: SiteQuality
SIO_000300: 1.555816e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2849
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5156
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 37051
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534118802160039e-5
allele num: 65184
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.021819348628268e-5
allele num: 12466
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.189e1

DP
type: SiteQuality
SIO_000300: 1.554273e6

FS
type: SiteQuality
SIO_000300: 2.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 8.25e1
variant carriers: 0