2-152496983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152496983
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152496983
    reference: chr 2
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8571G>A
  hgvsp: ENST00000603639.1:c.8571G>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.8571G>A
  hgvsp: ENST00000427231.2:c.8571G>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.8571G>A
  hgvsp: ENST00000172853.10:c.8571G>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.8571G>A
  hgvsp: ENST00000604864.1:c.8571G>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.8571G>A
  hgvsp: ENST00000397345.3:c.8571G>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.8571G>A
  hgvsp: ENST00000409198.1:c.8571G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys2857Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

2-152496986-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152496986
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152496986
    reference: chr 2
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
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.8568G>C
  hgvsp: ENSP00000380505.3:p.Lys2856Asn
  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.8568G>C
  hgvsp: ENSP00000416578.2:p.Lys2856Asn
  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.8568G>C
  hgvsp: ENSP00000172853.10:p.Lys2856Asn
  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.8568G>C
  hgvsp: ENSP00000474498.1:p.Lys2856Asn
  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.8568G>C
  hgvsp: ENSP00000473894.1:p.Lys2856Asn
  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.8568G>C
  hgvsp: ENSP00000386259.1:p.Lys2856Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15655
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys2856Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

2-152496994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152496994
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152496994
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
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.8560C>T
  hgvsp: ENST00000172853.10:c.8560C>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.8560C>T
  hgvsp: ENST00000604864.1:c.8560C>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.8560C>T
  hgvsp: ENST00000397345.3:c.8560C>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.8560C>T
  hgvsp: ENST00000409198.1:c.8560C>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.8560C>T
  hgvsp: ENST00000427231.2:c.8560C>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.8560C>T
  hgvsp: ENST00000603639.1:c.8560C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15653
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu2854Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

2-152496998-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152496998
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152496998
    reference: chr 2
allele count: 3
allele frequency: 2.484019474712682e-5
allele num: 120772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8556G>A
  hgvsp: ENST00000427231.2:c.8556G>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.8556G>A
  hgvsp: ENST00000603639.1:c.8556G>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.8556G>A
  hgvsp: ENST00000604864.1:c.8556G>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.8556G>A
  hgvsp: ENST00000397345.3:c.8556G>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.8556G>A
  hgvsp: ENST00000172853.10:c.8556G>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.8556G>A
  hgvsp: ENST00000409198.1:c.8556G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15655
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 21955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val2852Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

2-152497001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497001
    reference: chr 2
allele count: 36
allele frequency: 2.980774007650653e-4
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8553G>A
  hgvsp: ENST00000603639.1:c.8553G>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.8553G>A
  hgvsp: ENST00000397345.3:c.8553G>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.8553G>A
  hgvsp: ENST00000427231.2:c.8553G>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.8553G>A
  hgvsp: ENST00000409198.1:c.8553G>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.8553G>A
  hgvsp: ENST00000172853.10:c.8553G>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.8553G>A
  hgvsp: ENST00000604864.1:c.8553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3010
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly2851Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

2-152497017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497017
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497017
    reference: chr 2
allele count: 2
allele frequency: 1.656067832538421e-5
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8537C>T
  hgvsp: ENSP00000172853.10:p.Pro2846Leu
  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.8537C>T
  hgvsp: ENSP00000416578.2:p.Pro2846Leu
  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.8537C>T
  hgvsp: ENSP00000380505.3:p.Pro2846Leu
  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.8537C>T
  hgvsp: ENSP00000386259.1:p.Pro2846Leu
  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.8537C>T
  hgvsp: ENSP00000474498.1:p.Pro2846Leu
  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.8537C>T
  hgvsp: ENSP00000473894.1:p.Pro2846Leu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro2846Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-152497038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497038
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497038
    reference: chr 2
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8516G>A
  hgvsp: ENSP00000474498.1:p.Trp2839Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8516G>A
  hgvsp: ENSP00000172853.10:p.Trp2839Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8516G>A
  hgvsp: ENSP00000416578.2:p.Trp2839Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8516G>A
  hgvsp: ENSP00000386259.1:p.Trp2839Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8516G>A
  hgvsp: ENSP00000473894.1:p.Trp2839Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8516G>A
  hgvsp: ENSP00000380505.3:p.Trp2839Ter
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Trp2839Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

2-152497040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497040
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497040
    reference: chr 2
allele count: 2
allele frequency: 1.656095258599275e-5
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8514G>A
  hgvsp: ENST00000603639.1:c.8514G>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.8514G>A
  hgvsp: ENST00000604864.1:c.8514G>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.8514G>A
  hgvsp: ENST00000172853.10:c.8514G>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.8514G>A
  hgvsp: ENST00000409198.1:c.8514G>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.8514G>A
  hgvsp: ENST00000427231.2:c.8514G>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.8514G>A
  hgvsp: ENST00000397345.3:c.8514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3013
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys2838Lys
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-152497044-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497044
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497044
    reference: chr 2
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8510A>G
  hgvsp: ENSP00000473894.1:p.Glu2837Gly
  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.8510A>G
  hgvsp: ENSP00000172853.10:p.Glu2837Gly
  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.8510A>G
  hgvsp: ENSP00000386259.1:p.Glu2837Gly
  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.8510A>G
  hgvsp: ENSP00000474498.1:p.Glu2837Gly
  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.8510A>G
  hgvsp: ENSP00000380505.3:p.Glu2837Gly
  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.8510A>G
  hgvsp: ENSP00000416578.2:p.Glu2837Gly
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu2837Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

2-152497050-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497050
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497050
    reference: chr 2
allele count: 3
allele frequency: 2.484142887898912e-5
allele num: 120766
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.8504A>G
  hgvsp: ENSP00000386259.1:p.Asp2835Gly
  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.8504A>G
  hgvsp: ENSP00000172853.10:p.Asp2835Gly
  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.8504A>G
  hgvsp: ENSP00000380505.3:p.Asp2835Gly
  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.8504A>G
  hgvsp: ENSP00000473894.1:p.Asp2835Gly
  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.8504A>G
  hgvsp: ENSP00000474498.1:p.Asp2835Gly
  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.8504A>G
  hgvsp: ENSP00000416578.2:p.Asp2835Gly
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7248
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp2835Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-152497051-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497051
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497048
    reference: chr 2
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8500_8502delAAG
  hgvsp: ENSP00000474498.1:p.Lys2834del
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8500_8502delAAG
  hgvsp: ENSP00000380505.3:p.Lys2834del
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8500_8502delAAG
  hgvsp: ENSP00000386259.1:p.Lys2834del
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8500_8502delAAG
  hgvsp: ENSP00000473894.1:p.Lys2834del
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8500_8502delAAG
  hgvsp: ENSP00000172853.10:p.Lys2834del
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8500_8502delAAG
  hgvsp: ENSP00000416578.2:p.Lys2834del
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21972
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15627
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3014
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys2834del
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: CCTT
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

2-152497055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497055
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497055
    reference: chr 2
allele count: 180
allele frequency: 1.490485732739347e-3
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8499G>A
  hgvsp: ENST00000409198.1:c.8499G>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.8499G>A
  hgvsp: ENST00000397345.3:c.8499G>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.8499G>A
  hgvsp: ENST00000604864.1:c.8499G>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.8499G>A
  hgvsp: ENST00000172853.10:c.8499G>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.8499G>A
  hgvsp: ENST00000603639.1:c.8499G>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.8499G>A
  hgvsp: ENST00000427231.2:c.8499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 9.75e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3694
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4356
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21964
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys2833Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

2-152497064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497064
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497064
    reference: chr 2
allele count: 22
allele frequency: 1.821644448124534e-4
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8490G>A
  hgvsp: ENST00000603639.1:c.8490G>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.8490G>A
  hgvsp: ENST00000172853.10:c.8490G>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.8490G>A
  hgvsp: ENST00000397345.3:c.8490G>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.8490G>A
  hgvsp: ENST00000604864.1:c.8490G>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.8490G>A
  hgvsp: ENST00000409198.1:c.8490G>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.8490G>A
  hgvsp: ENST00000427231.2:c.8490G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7270
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15537
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 3016
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2830Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

2-152497069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497069
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497069
    reference: chr 2
allele count: 12
allele frequency: 9.936406995230525e-5
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8485G>A
  hgvsp: ENSP00000474498.1:p.Asp2829Asn
  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.8485G>A
  hgvsp: ENSP00000473894.1:p.Asp2829Asn
  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.8485G>A
  hgvsp: ENSP00000380505.3:p.Asp2829Asn
  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.8485G>A
  hgvsp: ENSP00000386259.1:p.Asp2829Asn
  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.8485G>A
  hgvsp: ENSP00000172853.10:p.Asp2829Asn
  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.8485G>A
  hgvsp: ENSP00000416578.2:p.Asp2829Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22041
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp2829Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

2-152497087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497087
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497087
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8467G>A
  hgvsp: ENSP00000474498.1:p.Val2823Met
  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.8467G>A
  hgvsp: ENSP00000473894.1:p.Val2823Met
  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.8467G>A
  hgvsp: ENSP00000172853.10:p.Val2823Met
  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.8467G>A
  hgvsp: ENSP00000416578.2:p.Val2823Met
  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.8467G>A
  hgvsp: ENSP00000386259.1:p.Val2823Met
  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.8467G>A
  hgvsp: ENSP00000380505.3:p.Val2823Met
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3703
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15514
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val2823Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-152497088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497088
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497088
    reference: chr 2
allele count: 2613
allele frequency: 2.163652623211447e-2
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8466C>T
  hgvsp: ENST00000604864.1:c.8466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8466C>T
  hgvsp: ENST00000427231.2:c.8466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8466C>T
  hgvsp: ENST00000172853.10:c.8466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8466C>T
  hgvsp: ENST00000603639.1:c.8466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8466C>T
  hgvsp: ENST00000409198.1:c.8466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8466C>T
  hgvsp: ENST00000397345.3:c.8466C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 9.75e1
  variant carriers: 2528
genotype depth: GenotypeDepth
  all individuals: 12889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2914
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16281
  bin: 9.75e1
  variant carriers: 2578
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His2822His
num of homozygotes: 35
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

2-152497088-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497088
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497088
    reference: chr 2
allele count: 2
allele frequency: 1.656067832538421e-5
allele num: 120768
alternate allele: C
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.8466C>G
  hgvsp: ENSP00000380505.3:p.His2822Gln
  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.8466C>G
  hgvsp: ENSP00000416578.2:p.His2822Gln
  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.8466C>G
  hgvsp: ENSP00000473894.1:p.His2822Gln
  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.8466C>G
  hgvsp: ENSP00000474498.1:p.His2822Gln
  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.8466C>G
  hgvsp: ENSP00000172853.10:p.His2822Gln
  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.8466C>G
  hgvsp: ENSP00000386259.1:p.His2822Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3631
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4284
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16281
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His2822Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-152497090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497090
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497090
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
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.8464C>T
  hgvsp: ENSP00000386259.1:p.His2822Tyr
  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.8464C>T
  hgvsp: ENSP00000172853.10:p.His2822Tyr
  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.8464C>T
  hgvsp: ENSP00000416578.2:p.His2822Tyr
  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.8464C>T
  hgvsp: ENSP00000474498.1:p.His2822Tyr
  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.8464C>T
  hgvsp: ENSP00000473894.1:p.His2822Tyr
  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.8464C>T
  hgvsp: ENSP00000380505.3:p.His2822Tyr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14326
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His2822Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/2-152497091-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497091
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497091
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
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.8463G>T
  hgvsp: ENSP00000416578.2:p.Met2821Ile
  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.8463G>T
  hgvsp: ENSP00000386259.1:p.Met2821Ile
  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.8463G>T
  hgvsp: ENSP00000473894.1:p.Met2821Ile
  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.8463G>T
  hgvsp: ENSP00000172853.10:p.Met2821Ile
  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.8463G>T
  hgvsp: ENSP00000380505.3:p.Met2821Ile
  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.8463G>T
  hgvsp: ENSP00000474498.1:p.Met2821Ile
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4467
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met2821Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

2-152497094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497094
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497094
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
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.8460C>T
  hgvsp: ENST00000172853.10:c.8460C>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.8460C>T
  hgvsp: ENST00000409198.1:c.8460C>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.8460C>T
  hgvsp: ENST00000603639.1:c.8460C>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.8460C>T
  hgvsp: ENST00000604864.1:c.8460C>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.8460C>T
  hgvsp: ENST00000427231.2:c.8460C>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.8460C>T
  hgvsp: ENST00000397345.3:c.8460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7479
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser2820Ser
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

2-152497094-GGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497094
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497092
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8458_8459delTC
  hgvsp: ENSP00000416578.2:p.Ser2820HisfsTer9
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8458_8459delTC
  hgvsp: ENSP00000380505.3:p.Ser2820HisfsTer9
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8458_8459delTC
  hgvsp: ENSP00000473894.1:p.Ser2820HisfsTer9
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8458_8459delTC
  hgvsp: ENSP00000386259.1:p.Ser2820HisfsTer9
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8458_8459delTC
  hgvsp: ENSP00000474498.1:p.Ser2820HisfsTer9
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8458_8459delTC
  hgvsp: ENSP00000172853.10:p.Ser2820HisfsTer9
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser2820HisfsTer9
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: GGA
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/2-152497119-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497119
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497119
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8435G>T
  hgvsp: ENSP00000380505.3:p.Arg2812Leu
  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.8435G>T
  hgvsp: ENSP00000416578.2:p.Arg2812Leu
  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.8435G>T
  hgvsp: ENSP00000386259.1:p.Arg2812Leu
  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.8435G>T
  hgvsp: ENSP00000473894.1:p.Arg2812Leu
  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.8435G>T
  hgvsp: ENSP00000172853.10:p.Arg2812Leu
  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.8435G>T
  hgvsp: ENSP00000474498.1:p.Arg2812Leu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14325
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2812Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

2-152497119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497119
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497119
    reference: chr 2
allele count: 3
allele frequency: 2.484225170169424e-5
allele num: 120762
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.8435G>A
  hgvsp: ENSP00000380505.3:p.Arg2812His
  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.8435G>A
  hgvsp: ENSP00000172853.10:p.Arg2812His
  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.8435G>A
  hgvsp: ENSP00000474498.1:p.Arg2812His
  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.8435G>A
  hgvsp: ENSP00000416578.2:p.Arg2812His
  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.8435G>A
  hgvsp: ENSP00000386259.1:p.Arg2812His
  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.8435G>A
  hgvsp: ENSP00000473894.1:p.Arg2812His
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14325
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg2812His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

2-152497120-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497120
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497120
    reference: chr 2
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
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.8434C>A
  hgvsp: ENSP00000380505.3:p.Arg2812Ser
  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.8434C>A
  hgvsp: ENSP00000473894.1:p.Arg2812Ser
  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.8434C>A
  hgvsp: ENSP00000416578.2:p.Arg2812Ser
  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.8434C>A
  hgvsp: ENSP00000172853.10:p.Arg2812Ser
  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.8434C>A
  hgvsp: ENSP00000386259.1:p.Arg2812Ser
  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.8434C>A
  hgvsp: ENSP00000474498.1:p.Arg2812Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7480
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg2812Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/2-152497128-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497128
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497128
    reference: chr 2
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8426G>T
  hgvsp: ENSP00000380505.3:p.Arg2809Leu
  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.8426G>T
  hgvsp: ENSP00000473894.1:p.Arg2809Leu
  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.8426G>T
  hgvsp: ENSP00000474498.1:p.Arg2809Leu
  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.8426G>T
  hgvsp: ENSP00000386259.1:p.Arg2809Leu
  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.8426G>T
  hgvsp: ENSP00000416578.2:p.Arg2809Leu
  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.8426G>T
  hgvsp: ENSP00000172853.10:p.Arg2809Leu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7478
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14322
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22709
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg2809Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

2-152497128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497128
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497128
    reference: chr 2
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
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.8426G>A
  hgvsp: ENSP00000380505.3:p.Arg2809Gln
  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.8426G>A
  hgvsp: ENSP00000474498.1:p.Arg2809Gln
  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.8426G>A
  hgvsp: ENSP00000172853.10:p.Arg2809Gln
  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.8426G>A
  hgvsp: ENSP00000416578.2:p.Arg2809Gln
  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.8426G>A
  hgvsp: ENSP00000473894.1:p.Arg2809Gln
  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.8426G>A
  hgvsp: ENSP00000386259.1:p.Arg2809Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22709
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14322
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg2809Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

2-152497129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497129
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497129
    reference: chr 2
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8425C>T
  hgvsp: ENSP00000172853.10:p.Arg2809Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8425C>T
  hgvsp: ENSP00000380505.3:p.Arg2809Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8425C>T
  hgvsp: ENSP00000386259.1:p.Arg2809Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8425C>T
  hgvsp: ENSP00000416578.2:p.Arg2809Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8425C>T
  hgvsp: ENSP00000474498.1:p.Arg2809Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8425C>T
  hgvsp: ENSP00000473894.1:p.Arg2809Ter
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22694
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14320
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3784
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg2809Ter
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

2-152497130-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497130
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497130
    reference: chr 2
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
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.8424C>T
  hgvsp: ENST00000603639.1:c.8424C>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.8424C>T
  hgvsp: ENST00000409198.1:c.8424C>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.8424C>T
  hgvsp: ENST00000172853.10:c.8424C>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.8424C>T
  hgvsp: ENST00000427231.2:c.8424C>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.8424C>T
  hgvsp: ENST00000397345.3:c.8424C>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.8424C>T
  hgvsp: ENST00000604864.1:c.8424C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8235
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14319
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala2808Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

2-152497132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497132
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497132
    reference: chr 2
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
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.8422G>A
  hgvsp: ENSP00000386259.1:p.Ala2808Thr
  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.8422G>A
  hgvsp: ENSP00000380505.3:p.Ala2808Thr
  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.8422G>A
  hgvsp: ENSP00000473894.1:p.Ala2808Thr
  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.8422G>A
  hgvsp: ENSP00000172853.10:p.Ala2808Thr
  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.8422G>A
  hgvsp: ENSP00000474498.1:p.Ala2808Thr
  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.8422G>A
  hgvsp: ENSP00000416578.2:p.Ala2808Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14314
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala2808Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

2-152497142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497142
    reference: chr 2
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
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.8412C>T
  hgvsp: ENST00000409198.1:c.8412C>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.8412C>T
  hgvsp: ENST00000603639.1:c.8412C>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.8412C>T
  hgvsp: ENST00000172853.10:c.8412C>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.8412C>T
  hgvsp: ENST00000397345.3:c.8412C>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.8412C>T
  hgvsp: ENST00000604864.1:c.8412C>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.8412C>T
  hgvsp: ENST00000427231.2:c.8412C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2749
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His2804His
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

2-152497143-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497143
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497143
    reference: chr 2
allele count: 1
allele frequency: 8.291873963515755e-6
allele num: 120600
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.8411A>G
  hgvsp: ENSP00000474498.1:p.His2804Arg
  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.8411A>G
  hgvsp: ENSP00000473894.1:p.His2804Arg
  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.8411A>G
  hgvsp: ENSP00000380505.3:p.His2804Arg
  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.8411A>G
  hgvsp: ENSP00000386259.1:p.His2804Arg
  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.8411A>G
  hgvsp: ENSP00000172853.10:p.His2804Arg
  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.8411A>G
  hgvsp: ENSP00000416578.2:p.His2804Arg
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His2804Arg
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-152497147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497147
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497147
    reference: chr 2
allele count: 1
allele frequency: 8.29324929507381e-6
allele num: 120580
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.8407G>A
  hgvsp: ENSP00000416578.2:p.Gly2803Ser
  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.8407G>A
  hgvsp: ENSP00000473894.1:p.Gly2803Ser
  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.8407G>A
  hgvsp: ENSP00000386259.1:p.Gly2803Ser
  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.8407G>A
  hgvsp: ENSP00000172853.10:p.Gly2803Ser
  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.8407G>A
  hgvsp: ENSP00000380505.3:p.Gly2803Ser
  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.8407G>A
  hgvsp: ENSP00000474498.1:p.Gly2803Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2749
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly2803Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

2-152497148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497148
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497148
    reference: chr 2
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
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.8406C>T
  hgvsp: ENST00000427231.2:c.8406C>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.8406C>T
  hgvsp: ENST00000603639.1:c.8406C>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.8406C>T
  hgvsp: ENST00000397345.3:c.8406C>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.8406C>T
  hgvsp: ENST00000604864.1:c.8406C>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.8406C>T
  hgvsp: ENST00000172853.10:c.8406C>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.8406C>T
  hgvsp: ENST00000409198.1:c.8406C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7452
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu2802Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-152497149-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497149
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497150
    reference: chr 2
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: AG
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8404dupC
  hgvsp: ENSP00000380505.3:p.Leu2802ProfsTer12
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8404dupC
  hgvsp: ENSP00000172853.10:p.Leu2802ProfsTer12
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8404dupC
  hgvsp: ENSP00000386259.1:p.Leu2802ProfsTer12
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8404dupC
  hgvsp: ENSP00000473894.1:p.Leu2802ProfsTer12
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8404dupC
  hgvsp: ENSP00000416578.2:p.Leu2802ProfsTer12
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8404dupC
  hgvsp: ENSP00000474498.1:p.Leu2802ProfsTer12
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7444
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu2802ProfsTer12
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-152497149-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497149
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497149
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 120518
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.8405T>C
  hgvsp: ENSP00000172853.10:p.Leu2802Pro
  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.8405T>C
  hgvsp: ENSP00000380505.3:p.Leu2802Pro
  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.8405T>C
  hgvsp: ENSP00000474498.1:p.Leu2802Pro
  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.8405T>C
  hgvsp: ENSP00000416578.2:p.Leu2802Pro
  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.8405T>C
  hgvsp: ENSP00000386259.1:p.Leu2802Pro
  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.8405T>C
  hgvsp: ENSP00000473894.1:p.Leu2802Pro
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu2802Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

2-152497156-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497156
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497156
    reference: chr 2
allele count: 2
allele frequency: 1.657247974014352e-5
allele num: 120682
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.8398A>G
  hgvsp: ENSP00000474498.1:p.Lys2800Glu
  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.8398A>G
  hgvsp: ENSP00000473894.1:p.Lys2800Glu
  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.8398A>G
  hgvsp: ENSP00000380505.3:p.Lys2800Glu
  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.8398A>G
  hgvsp: ENSP00000172853.10:p.Lys2800Glu
  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.8398A>G
  hgvsp: ENSP00000416578.2:p.Lys2800Glu
  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.8398A>G
  hgvsp: ENSP00000386259.1:p.Lys2800Glu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8232
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4458
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys2800Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

2-152497158-C-CGATA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497158
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497162
    reference: chr 2
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: CGATA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8392_8395dupTATC
  hgvsp: ENSP00000473894.1:p.Arg2799LeufsTer3
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8392_8395dupTATC
  hgvsp: ENSP00000172853.10:p.Arg2799LeufsTer3
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8392_8395dupTATC
  hgvsp: ENSP00000386259.1:p.Arg2799LeufsTer3
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8392_8395dupTATC
  hgvsp: ENSP00000416578.2:p.Arg2799LeufsTer3
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8392_8395dupTATC
  hgvsp: ENSP00000474498.1:p.Arg2799LeufsTer3
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8392_8395dupTATC
  hgvsp: ENSP00000380505.3:p.Arg2799LeufsTer3
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14325
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg2799LeufsTer3
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

2-152497158-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497158
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497158
    reference: chr 2
allele count: 3
allele frequency: 2.486407638244265e-5
allele num: 120656
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.8396G>A
  hgvsp: ENSP00000416578.2:p.Arg2799His
  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.8396G>A
  hgvsp: ENSP00000380505.3:p.Arg2799His
  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.8396G>A
  hgvsp: ENSP00000386259.1:p.Arg2799His
  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.8396G>A
  hgvsp: ENSP00000172853.10:p.Arg2799His
  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.8396G>A
  hgvsp: ENSP00000473894.1:p.Arg2799His
  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.8396G>A
  hgvsp: ENSP00000474498.1:p.Arg2799His
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14325
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7463
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3775
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg2799His
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

2-152497159-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497159
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497159
    reference: chr 2
allele count: 2
allele frequency: 1.657605092162843e-5
allele num: 120656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8395C>T
  hgvsp: ENSP00000172853.10:p.Arg2799Cys
  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.8395C>T
  hgvsp: ENSP00000416578.2:p.Arg2799Cys
  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.8395C>T
  hgvsp: ENSP00000474498.1:p.Arg2799Cys
  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.8395C>T
  hgvsp: ENSP00000473894.1:p.Arg2799Cys
  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.8395C>T
  hgvsp: ENSP00000380505.3:p.Arg2799Cys
  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.8395C>T
  hgvsp: ENSP00000386259.1:p.Arg2799Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22639
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14322
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg2799Cys
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

2-152497161-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497161
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497161
    reference: chr 2
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
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.8393A>G
  hgvsp: ENSP00000172853.10:p.Tyr2798Cys
  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.8393A>G
  hgvsp: ENSP00000473894.1:p.Tyr2798Cys
  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.8393A>G
  hgvsp: ENSP00000386259.1:p.Tyr2798Cys
  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.8393A>G
  hgvsp: ENSP00000474498.1:p.Tyr2798Cys
  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.8393A>G
  hgvsp: ENSP00000380505.3:p.Tyr2798Cys
  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.8393A>G
  hgvsp: ENSP00000416578.2:p.Tyr2798Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14322
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22573
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr2798Cys
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-152497167-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497167
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497167
    reference: chr 2
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
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.8387A>G
  hgvsp: ENSP00000474498.1:p.Glu2796Gly
  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.8387A>G
  hgvsp: ENSP00000172853.10:p.Glu2796Gly
  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.8387A>G
  hgvsp: ENSP00000473894.1:p.Glu2796Gly
  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.8387A>G
  hgvsp: ENSP00000386259.1:p.Glu2796Gly
  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.8387A>G
  hgvsp: ENSP00000380505.3:p.Glu2796Gly
  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.8387A>G
  hgvsp: ENSP00000416578.2:p.Glu2796Gly
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3772
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu2796Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

2-152497173-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497173
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497173
    reference: chr 2
allele count: 2
allele frequency: 1.664530519167069e-5
allele num: 120154
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.8381A>T
  hgvsp: ENSP00000386259.1:p.Tyr2794Phe
  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.8381A>T
  hgvsp: ENSP00000416578.2:p.Tyr2794Phe
  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.8381A>T
  hgvsp: ENSP00000380505.3:p.Tyr2794Phe
  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.8381A>T
  hgvsp: ENSP00000473894.1:p.Tyr2794Phe
  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.8381A>T
  hgvsp: ENSP00000172853.10:p.Tyr2794Phe
  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.8381A>T
  hgvsp: ENSP00000474498.1:p.Tyr2794Phe
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1817
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7385
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr2794Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

2-152497177-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497177
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497177
    reference: chr 2
allele count: 1
allele frequency: 8.335834083558401e-6
allele num: 119964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8377A>G
  hgvsp: ENSP00000416578.2:p.Lys2793Glu
  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.8377A>G
  hgvsp: ENSP00000172853.10:p.Lys2793Glu
  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.8377A>G
  hgvsp: ENSP00000386259.1:p.Lys2793Glu
  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.8377A>G
  hgvsp: ENSP00000474498.1:p.Lys2793Glu
  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.8377A>G
  hgvsp: ENSP00000473894.1:p.Lys2793Glu
  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.8377A>G
  hgvsp: ENSP00000380505.3:p.Lys2793Glu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14319
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys2793Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

2-152497190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497190
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497190
    reference: chr 2
allele count: 1
allele frequency: 8.429570934839416e-6
allele num: 118630
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.8374-10C>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.8374-10C>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.8374-10C>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.8374-10C>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.8374-10C>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.8374-10C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13099
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6957
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14308
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19843
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2520
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4386
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-152497198-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497198
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497198
    reference: chr 2
allele count: 2
allele frequency: 1.698802344347235e-5
allele num: 117730
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8374-18G>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.8374-18G>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.8374-18G>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.8374-18G>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.8374-18G>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.8374-18G>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3751
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14307
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

2-152497198-CAGAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497198
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497194
    reference: chr 2
allele count: 1
allele frequency: 8.494011721736177e-6
allele num: 117730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8374-22_8374-19delATCT
  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.8374-22_8374-19delATCT
  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.8374-22_8374-19delATCT
  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.8374-22_8374-19delATCT
  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.8374-22_8374-19delATCT
  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.8374-22_8374-19delATCT
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4370
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3751
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6772
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: CAGAT
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

2-152497202-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497202
    reference: chr 2
allele count: 1
allele frequency: 8.536939336509074e-6
allele num: 117138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8374-22A>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.8374-22A>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.8374-22A>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.8374-22A>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.8374-22A>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.8374-22A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8031
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16467
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3017
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6580
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14305
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

2-152497209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497209
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497209
    reference: chr 2
allele count: 1
allele frequency: 8.606000103272e-6
allele num: 116198
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.8374-29G>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.8374-29G>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.8374-29G>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.8374-29G>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.8374-29G>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.8374-29G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6271
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4631
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4329
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3743
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

2-152497211-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497211
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497211
    reference: chr 2
allele count: 1
allele frequency: 8.615490652192642e-6
allele num: 116070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8374-31C>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.8374-31C>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.8374-31C>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.8374-31C>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.8374-31C>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.8374-31C>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3738
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 1774
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

2-152497218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497218
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497218
    reference: chr 2
allele count: 34
allele frequency: 2.962395009235702e-4
allele num: 114772
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.8374-38G>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.8374-38G>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.8374-38G>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.8374-38G>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.8374-38G>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.8374-38G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10615
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14314
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12250
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-152497221-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497221
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497221
    reference: chr 2
allele count: 5
allele frequency: 4.369330793295699e-5
allele num: 114434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8374-41A>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.8374-41A>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.8374-41A>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.8374-41A>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.8374-41A>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.8374-41A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10236
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5385
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

2-152497224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497224
    reference: chr 2
allele count: 2
allele frequency: 1.758025385886572e-5
allele num: 113764
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.8374-44C>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.8374-44C>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.8374-44C>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.8374-44C>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.8374-44C>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.8374-44C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3008
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5126
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3640
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14287
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD

2-152497224-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497224
    reference: chr 2
allele count: 1
allele frequency: 8.790126929432861e-6
allele num: 113764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8374-44C>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.8374-44C>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.8374-44C>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.8374-44C>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.8374-44C>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.8374-44C>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9229
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3709
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3008
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5126
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

2-152497229-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152497229
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152497229
    reference: chr 2
allele count: 1
allele frequency: 8.86037816093991e-6
allele num: 112862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8374-49T>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.8374-49T>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.8374-49T>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.8374-49T>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.8374-49T>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.8374-49T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8867
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2946
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2523
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4153
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-152499051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499051
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499051
    reference: chr 2
allele count: 1
allele frequency: 1.010325526884762e-5
allele num: 98978
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.8373+37G>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.8373+37G>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.8373+37G>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.8373+37G>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.8373+37G>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.8373+37G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14622
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15703
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3148
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

2-152499056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499056
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499056
    reference: chr 2
allele count: 9
allele frequency: 8.958789567987259e-5
allele num: 100460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8373+32C>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.8373+32C>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.8373+32C>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.8373+32C>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.8373+32C>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.8373+32C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10016
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6861
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4799
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4105
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-152499062-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499062
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499063
    reference: chr 2
allele count: 3
allele frequency: 2.913979330173285e-5
allele num: 102952
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8373+25_8373+26insT
  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.8373+25_8373+26insT
  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.8373+25_8373+26insT
  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.8373+25_8373+26insT
  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.8373+25_8373+26insT
  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.8373+25_8373+26insT
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27079
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9020
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4960
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3250
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/2-152499063-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499063
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499063
    reference: chr 2
allele count: 3
allele frequency: 2.900007733353956e-5
allele num: 103448
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.8373+25G>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.8373+25G>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.8373+25G>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.8373+25G>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.8373+25G>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.8373+25G>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28046
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30197
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8680
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3046
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

2-152499072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499072
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499072
    reference: chr 2
allele count: 2
allele frequency: 1.835199119104423e-5
allele num: 108980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8373+16A>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.8373+16A>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.8373+16A>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.8373+16A>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.8373+16A>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.8373+16A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

2-152499073-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499073
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499073
    reference: chr 2
allele count: 2
allele frequency: 1.826283877565929e-5
allele num: 109512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8373+15A>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.8373+15A>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.8373+15A>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.8373+15A>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.8373+15A>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.8373+15A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36443
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39686
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

2-152499075-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499075
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499075
    reference: chr 2
allele count: 37
allele frequency: 3.343212375307214e-4
allele num: 110672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8373+13G>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.8373+13G>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.8373+13G>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.8373+13G>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.8373+13G>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.8373+13G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37354
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40818
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 9.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

2-152499080-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499080
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499080
    reference: chr 2
allele count: 1
allele frequency: 8.802971883307805e-6
allele num: 113598
alternate allele: G
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.8373+8T>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.8373+8T>C
  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.8373+8T>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.8373+8T>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.8373+8T>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.8373+8T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
hgvs: c.8373+8T>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/2-152499086-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499086
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499086
    reference: chr 2
allele count: 1
allele frequency: 8.601262665359275e-6
allele num: 116262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.8373+2T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.8373+2T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8373+2T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.8373+2T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.8373+2T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.8373+2T>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.25e1
  variant carriers: 0
hgvs: c.8373+2T>G
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

2-152499101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499101
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499101
    reference: chr 2
allele count: 1
allele frequency: 8.400678774845007e-6
allele num: 119038
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.8360A>G
  hgvsp: ENSP00000380505.3:p.Asp2787Gly
  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.8360A>G
  hgvsp: ENSP00000386259.1:p.Asp2787Gly
  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.8360A>G
  hgvsp: ENSP00000172853.10:p.Asp2787Gly
  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.8360A>G
  hgvsp: ENSP00000474498.1:p.Asp2787Gly
  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.8360A>G
  hgvsp: ENSP00000416578.2:p.Asp2787Gly
  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.8360A>G
  hgvsp: ENSP00000473894.1:p.Asp2787Gly
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3159
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp2787Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-152499102-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499102
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499102
    reference: chr 2
allele count: 6
allele frequency: 5.036430178289628e-5
allele num: 119132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8359G>T
  hgvsp: ENSP00000473894.1:p.Asp2787Tyr
  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.8359G>T
  hgvsp: ENSP00000380505.3:p.Asp2787Tyr
  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.8359G>T
  hgvsp: ENSP00000172853.10:p.Asp2787Tyr
  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.8359G>T
  hgvsp: ENSP00000386259.1:p.Asp2787Tyr
  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.8359G>T
  hgvsp: ENSP00000416578.2:p.Asp2787Tyr
  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.8359G>T
  hgvsp: ENSP00000474498.1:p.Asp2787Tyr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp2787Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

2-152499102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499102
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499102
    reference: chr 2
allele count: 4
allele frequency: 3.357620118859753e-5
allele num: 119132
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.8359G>A
  hgvsp: ENSP00000172853.10:p.Asp2787Asn
  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.8359G>A
  hgvsp: ENSP00000380505.3:p.Asp2787Asn
  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.8359G>A
  hgvsp: ENSP00000416578.2:p.Asp2787Asn
  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.8359G>A
  hgvsp: ENSP00000473894.1:p.Asp2787Asn
  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.8359G>A
  hgvsp: ENSP00000386259.1:p.Asp2787Asn
  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.8359G>A
  hgvsp: ENSP00000474498.1:p.Asp2787Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9970
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3166
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp2787Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-152499105-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499105
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499105
    reference: chr 2
allele count: 16
allele frequency: 1.340033500837521e-4
allele num: 119400
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.8356A>G
  hgvsp: ENSP00000380505.3:p.Arg2786Gly
  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.8356A>G
  hgvsp: ENSP00000474498.1:p.Arg2786Gly
  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.8356A>G
  hgvsp: ENSP00000386259.1:p.Arg2786Gly
  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.8356A>G
  hgvsp: ENSP00000172853.10:p.Arg2786Gly
  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.8356A>G
  hgvsp: ENSP00000473894.1:p.Arg2786Gly
  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.8356A>G
  hgvsp: ENSP00000416578.2:p.Arg2786Gly
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg2786Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

2-152499111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499111
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499111
    reference: chr 2
allele count: 18
allele frequency: 1.502880520998581e-4
allele num: 119770
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.8350G>A
  hgvsp: ENSP00000473894.1:p.Ala2784Thr
  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.8350G>A
  hgvsp: ENSP00000386259.1:p.Ala2784Thr
  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.8350G>A
  hgvsp: ENSP00000416578.2:p.Ala2784Thr
  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.8350G>A
  hgvsp: ENSP00000474498.1:p.Ala2784Thr
  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.8350G>A
  hgvsp: ENSP00000172853.10:p.Ala2784Thr
  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.8350G>A
  hgvsp: ENSP00000380505.3:p.Ala2784Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10321
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala2784Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-152499126-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499126
    reference: chr 2
allele count: 307
allele frequency: 2.554629121107727e-3
allele num: 120174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.8335A>G
  hgvsp: ENSP00000473894.1:p.Ile2779Val
  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.8335A>G
  hgvsp: ENSP00000416578.2:p.Ile2779Val
  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.8335A>G
  hgvsp: ENSP00000380505.3:p.Ile2779Val
  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.8335A>G
  hgvsp: ENSP00000474498.1:p.Ile2779Val
  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.8335A>G
  hgvsp: ENSP00000386259.1:p.Ile2779Val
  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.8335A>G
  hgvsp: ENSP00000172853.10:p.Ile2779Val
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42913
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10632
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile2779Val
num of homozygotes: 12
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-152499133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499133
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499133
    reference: chr 2
allele count: 7
allele frequency: 5.823821092216047e-5
allele num: 120196
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.8328C>T
  hgvsp: ENST00000604864.1:c.8328C>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.8328C>T
  hgvsp: ENST00000409198.1:c.8328C>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.8328C>T
  hgvsp: ENST00000603639.1:c.8328C>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.8328C>T
  hgvsp: ENST00000397345.3:c.8328C>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.8328C>T
  hgvsp: ENST00000427231.2:c.8328C>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.8328C>T
  hgvsp: ENST00000172853.10:c.8328C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 9.75e1
  variant carriers: 7
hgvs: p.Ala2776Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

2-152499137-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499137
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499137
    reference: chr 2
allele count: 2
allele frequency: 1.6641427168794e-5
allele num: 120182
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.8324A>T
  hgvsp: ENSP00000474498.1:p.Asp2775Val
  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.8324A>T
  hgvsp: ENSP00000473894.1:p.Asp2775Val
  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.8324A>T
  hgvsp: ENSP00000172853.10:p.Asp2775Val
  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.8324A>T
  hgvsp: ENSP00000380505.3:p.Asp2775Val
  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.8324A>T
  hgvsp: ENSP00000416578.2:p.Asp2775Val
  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.8324A>T
  hgvsp: ENSP00000386259.1:p.Asp2775Val
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50017
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp2775Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-152499142-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499142
    reference: chr 2
allele count: 2
allele frequency: 1.665112561609165e-5
allele num: 120112
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.8319G>T
  hgvsp: ENST00000604864.1:c.8319G>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.8319G>T
  hgvsp: ENST00000172853.10:c.8319G>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.8319G>T
  hgvsp: ENST00000397345.3:c.8319G>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.8319G>T
  hgvsp: ENST00000409198.1:c.8319G>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.8319G>T
  hgvsp: ENST00000427231.2:c.8319G>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.8319G>T
  hgvsp: ENST00000603639.1:c.8319G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3808
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2773Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-152499143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152499143
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152499143
    reference: chr 2
allele count: 2834
allele frequency: 2.358875330858484e-2
allele num: 120142
alternate allele: T
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.8318G>A
  hgvsp: ENSP00000386259.1:p.Arg2773Gln
  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.8318G>A
  hgvsp: ENSP00000416578.2:p.Arg2773Gln
  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.8318G>A
  hgvsp: ENSP00000380505.3:p.Arg2773Gln
  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.8318G>A
  hgvsp: ENSP00000474498.1:p.Arg2773Gln
  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.8318G>A
  hgvsp: ENSP00000172853.10:p.Arg2773Gln
  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.8318G>A
  hgvsp: ENSP00000473894.1:p.Arg2773Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.75e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 40765
  bin: 2.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 3.25e1
  variant carriers: 242
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.25e1
  variant carriers: 251
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 353
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 2.75e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 312
hgvs: p.Arg2773Gln
num of homozygotes: 37
reference allele: C

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

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15655
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3012
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21954
bin: 6.25e1
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: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.663e1

VQSLOD
type: SiteQuality
SIO_000300: -1.09e0

DP
type: SiteQuality
SIO_000300: 2.240343e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-1

FS
type: SiteQuality
SIO_000300: 4.279e0

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
all individuals: 4360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7244
bin: 6.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.725e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.435e0

QD
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: -1.453e1

FS
type: SiteQuality
SIO_000300: 4.841e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.679e0

DP
type: SiteQuality
SIO_000300: 2.240239e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.344e0

GenotypeQuality
all individuals: 21955
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7243
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3698
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
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: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.316e0

MQ
type: SiteQuality
SIO_000300: 4.804e1

MQRankSum
type: SiteQuality
SIO_000300: -4.793e0

VQSLOD
type: SiteQuality
SIO_000300: -4.163e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.36e-1

QD
type: SiteQuality
SIO_000300: 7.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 4.923e0

DP
type: SiteQuality
SIO_000300: 2.240458e6

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

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3013
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
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: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.542e0

MQ
type: SiteQuality
SIO_000300: 4.979e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.240893e6

VQSLOD
type: SiteQuality
SIO_000300: -1.138e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.322e0

QD
type: SiteQuality
SIO_000300: 1.269e1

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

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

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21957
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15660
bin: 9.75e1
variant carriers: 36

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

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

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

GenotypeQuality
all individuals: 0
bin: 5.75e1
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: 30
allele frequency: 3.058727569331158e-3
allele num: 9808
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.744e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 5.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -7.518e-1

DP
type: SiteQuality
SIO_000300: 2.247559e6

QD
type: SiteQuality
SIO_000300: 1.405e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

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

GenotypeQuality
all individuals: 21966
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7248
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3700
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4363
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15634
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.313e0

MQ
type: SiteQuality
SIO_000300: 4.56e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.214e0

DP
type: SiteQuality
SIO_000300: 2.239765e6

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21969
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15632
bin: 9.75e1
variant carriers: 1

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: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 8626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

DP
type: SiteQuality
SIO_000300: 2.239443e6

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.64e0

QD
type: SiteQuality
SIO_000300: 1.12e1

FS
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 4.44e1

VQSLOD
type: SiteQuality
SIO_000300: -2.158e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.91e-1

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 15631
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 4.432e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.211e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.537e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 2.239641e6

GenotypeQuality
all individuals: 15630
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3013
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4363
bin: 7.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 66740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.351e0

MQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.886e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 2.239337e6

VQSLOD
type: SiteQuality
SIO_000300: -1.695e0

MQ
type: SiteQuality
SIO_000300: 4.531e1

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4363
bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

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

Latino
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allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.065e1

MQ
type: SiteQuality
SIO_000300: 4.602e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

FS
type: SiteQuality
SIO_000300: 3.236e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

VQSLOD
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SIO_000300: -1.712e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.23997e6

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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bin: 5.25e1
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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bin: 7.75e1
variant carriers: 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: 8626
num of homozygotes: 0

Latino
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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: 66740
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.4e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
SIO_000300: 1.585e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.998e0

FS
type: SiteQuality
SIO_000300: 3.462e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.05e-1

DP
type: SiteQuality
SIO_000300: 2.239409e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 180

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

East Asian
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allele count: 167
allele frequency: 1.936007419429631e-2
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
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South Asian
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allele count: 13
allele frequency: 7.873062015503876e-4
allele num: 16512
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.435e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQ
type: SiteQuality
SIO_000300: 4.356e1

DP
type: SiteQuality
SIO_000300: 2.286139e6

MQRankSum
type: SiteQuality
SIO_000300: -7.078e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.996e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.296373988612526e-4
allele num: 66740
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 4.825e1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.240912e6

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

QD
type: SiteQuality
SIO_000300: 1.175e1

FS
type: SiteQuality
SIO_000300: 1.828e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.74e0

GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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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: 3016
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
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

South Asian
type: Population
allele count: 12
allele frequency: 7.267441860465116e-4
allele num: 16512
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.413e0

QD
type: SiteQuality
SIO_000300: 1.162e1

MQ
type: SiteQuality
SIO_000300: 4.872e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.23923e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.548999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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: 0
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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: 898
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 11576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.047e0

MQRankSum
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SIO_000300: 1.44e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.56e-1

MQ
type: SiteQuality
SIO_000300: 5.405e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

DP
type: SiteQuality
SIO_000300: 2.236187e6

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

Other
type: Population
allele count: 10
allele frequency: 1.11358574610245e-2
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 31
allele frequency: 3.593786227683747e-3
allele num: 8626
num of homozygotes: 0

European (Finnish)
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allele count: 85
allele frequency: 1.285152706380405e-2
allele num: 6614
num of homozygotes: 1

African
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allele count: 459
allele frequency: 4.682717812691287e-2
allele num: 9802
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South Asian
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allele count: 743
allele frequency: 4.499757751937984e-2
allele num: 16512
num of homozygotes: 18

European (Non-Finnish)
type: Population
allele count: 1178
allele frequency: 1.765058435720707e-2
allele num: 66740
num of homozygotes: 6

Latino
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allele count: 107
allele frequency: 9.243261921216309e-3
allele num: 11576
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.248e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.118e0

FS
type: SiteQuality
SIO_000300: 2.825e0

InbreedingCoeff
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SIO_000300: 7.2e-3

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.991e1

MQRankSum
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SIO_000300: -4.269e0

VQSLOD
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
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allele frequency: 0.0e0
allele num: 9802
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

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

Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66740
num of homozygotes: 0

South Asian
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Latino
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East Asian
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FS
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
type: Population
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Other
type: Population
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

East Asian
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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QD
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DP
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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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

DP
type: SiteQuality
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MQ
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BaseQRankSum
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SIO_000300: -5.09e-1

QD
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InbreedingCoeff
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SIO_000300: 2.5e-3

VQSLOD
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 4.147e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

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

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.389e1

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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DP
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SIO_000300: 2.19816e6

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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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 9802
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 5.659999999999999e-1

QD
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FS
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DP
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VQSLOD
type: SiteQuality
SIO_000300: -9.582000000000001e-1

InbreedingCoeff
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SIO_000300: 4.8e-3

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

African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
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DP
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ReadPosRankSum
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SIO_000300: -3.85e-1

FS
type: SiteQuality
SIO_000300: 1.743e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.273e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

QD
type: SiteQuality
SIO_000300: 1.433e1

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

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

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

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

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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FS
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SIO_000300: 2.012e0

ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
type: SiteQuality
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66732
num of homozygotes: 0

InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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MQ
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DP
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ClippingRankSum
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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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Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66730
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African
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South Asian
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East Asian
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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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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African
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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South Asian
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allele num: 16512
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East Asian
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BaseQRankSum
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SIO_000300: -1.266e0

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

Other
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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East Asian
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European (Finnish)
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African
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Latino
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

VQSLOD
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SIO_000300: -1.031e0

BaseQRankSum
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QD
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ClippingRankSum
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.26e0

ReadPosRankSum
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SIO_000300: -7.92e-1

MQ
type: SiteQuality
SIO_000300: 5.462e1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.194068e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

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

MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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DP
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ClippingRankSum
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MQ
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BaseQRankSum
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SIO_000300: -9.191000000000001e0

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

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

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

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

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

DP
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SIO_000300: 2.193512e6

ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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MQRankSum
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SIO_000300: 3.15e0

ClippingRankSum
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QD
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VQSLOD
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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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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

DP
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SIO_000300: 2.193605e6

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.5674e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.034e0

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
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SIO_000300: 1.38e0

VQSLOD
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InbreedingCoeff
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.666e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.249e0

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: 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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Finnish)
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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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.5674e1

MQ
type: SiteQuality
SIO_000300: 5.666e1

VQSLOD
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SIO_000300: -4.997e0

ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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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bin: 9.75e1
variant carriers: 2

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

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

Latino
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allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

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

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

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

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

East Asian
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num of homozygotes: 0

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

Other
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Latino
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European (Non-Finnish)
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allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

BaseQRankSum
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MQ
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VQSLOD
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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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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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 1.819284414796847e-4
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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Other
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Latino
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African
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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MQ
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FS
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 66664
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Latino
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FS
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ClippingRankSum
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QD
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.193518e6

VQSLOD
type: SiteQuality
SIO_000300: -8.648e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.81e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.602e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.606e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.443e0

DP
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SIO_000300: 2.191025e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.2e0

MQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e0

MQ
type: SiteQuality
SIO_000300: 5.409e1

QD
type: SiteQuality
SIO_000300: 1.574e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.562e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

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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variant carriers: 2

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

South Asian
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allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.009962977455377e-5
allele num: 66446
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.258e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.184638e6

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

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

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

East Asian
type: Population
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allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.341e1

QD
type: SiteQuality
SIO_000300: 1.261e1

VQSLOD
type: SiteQuality
SIO_000300: -1.313e0

DP
type: SiteQuality
SIO_000300: 2.180619e6

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
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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: 131
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variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519710647092794e-5
allele num: 65802
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15636
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

DP
type: SiteQuality
SIO_000300: 2.147892e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.111e1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.568e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 31
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3017
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 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: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.05791694697572e-5
allele num: 65404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.882e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 1.2243e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

QD
type: SiteQuality
SIO_000300: 1.568e1

MQ
type: SiteQuality
SIO_000300: 5.481e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 2.121342e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65404
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.521455588887439e-5
allele num: 15334
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.882e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
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SIO_000300: 1.2243e1

ReadPosRankSum
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DP
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MQRankSum
type: SiteQuality
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VQSLOD
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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bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65092
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.574621959237344e-5
allele num: 15210
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.255e-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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variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.700616456714018e-5
allele num: 14924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11422
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

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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African
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 14900
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Other
type: Population
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Latino
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
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QD
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DP
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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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.151260504201681e-4
allele num: 9520
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 1
allele frequency: 1.17096018735363e-3
allele num: 854
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European (Non-Finnish)
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allele count: 30
allele frequency: 4.692045418999656e-4
allele num: 63938
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6578
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Latino
type: Population
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

QD
type: SiteQuality
SIO_000300: 1.431e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.554e0

DP
type: SiteQuality
SIO_000300: 2.011315e6

MQ
type: SiteQuality
SIO_000300: 5.564e1

GenotypeQuality
all individuals: 1238
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3009
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14287
bin: 9.75e1
variant carriers: 5

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63800
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.222000995520159e-4
allele num: 8036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.216e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.71e0

MQ
type: SiteQuality
SIO_000300: 5.607e1

QD
type: SiteQuality
SIO_000300: 1.704e1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.997787e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

GenotypeQuality
all individuals: 1224
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1805
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3709
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.150995714645828e-5
allele num: 63472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.027e0

MQ
type: SiteQuality
SIO_000300: 5.526e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.394e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.984719e6

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-2

GenotypeQuality
all individuals: 14287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 583
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3640
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575497857322914e-5
allele num: 63472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14124
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.394e1

DP
type: SiteQuality
SIO_000300: 1.984719e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.027e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

MQ
type: SiteQuality
SIO_000300: 5.526e1

GenotypeQuality
all individuals: 2948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14286
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6101
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.587603988061218e-5
allele num: 62988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.777e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.071e1

DP
type: SiteQuality
SIO_000300: 1.97215e6

VQSLOD
type: SiteQuality
SIO_000300: -1.697e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

GenotypeQuality
all individuals: 2478
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8085
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.810413498443044e-5
allele num: 55236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12218
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

DP
type: SiteQuality
SIO_000300: 1.146426e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 1.349e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.171e0

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

GenotypeQuality
all individuals: 613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 1.040703052728955e-3
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56044
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.717e0

DP
type: SiteQuality
SIO_000300: 1.204176e6

VQSLOD
type: SiteQuality
SIO_000300: 5.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.487e1

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.222477543346563e-5
allele num: 57444
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.196e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

DP
type: SiteQuality
SIO_000300: 1.278583e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.85e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 808
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 197
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.196424859696528e-5
allele num: 57732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12946
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.294145e6

VQSLOD
type: SiteQuality
SIO_000300: -7.318e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.23e-1

MQ
type: SiteQuality
SIO_000300: 6.008e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.988e0

QD
type: SiteQuality
SIO_000300: 1.805e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e-1

GenotypeQuality
all individuals: 39033
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 3148
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6111
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.285366975491162e-5
allele num: 60876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13712
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.787e0

MQRankSum
type: SiteQuality
SIO_000300: -2.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

DP
type: SiteQuality
SIO_000300: 1.391101e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.634e1

GenotypeQuality
all individuals: 3149
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.255840951966333e-5
allele num: 13782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634360801490537e-5
allele num: 61186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.038e1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 2.673e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.400015e6

GenotypeQuality
all individuals: 2940
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5119
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
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variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.514747859181732e-5
allele num: 10510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

African
type: Population
allele count: 36
allele frequency: 3.926701570680628e-3
allele num: 9168
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

FS
type: SiteQuality
SIO_000300: 7.52e-1

DP
type: SiteQuality
SIO_000300: 1.421632e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

GenotypeQuality
all individuals: 3224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575348939790164e-5
allele num: 63478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
SIO_000300: 4.312e0

VQSLOD
type: SiteQuality
SIO_000300: -1.454e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

QD
type: SiteQuality
SIO_000300: 1.765e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

DP
type: SiteQuality
SIO_000300: 1.459624e6

GenotypeQuality
all individuals: 3400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46940
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.536570374923171e-4
allele num: 6508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64842
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -2.434e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

DP
type: SiteQuality
SIO_000300: 1.494623e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 1.653e1

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.0351966873706e-4
allele num: 9660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66114
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

QD
type: SiteQuality
SIO_000300: 1.577e1

VQSLOD
type: SiteQuality
SIO_000300: -1.289e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 1.272e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.31e0

DP
type: SiteQuality
SIO_000300: 1.531075e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

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

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 805
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66136
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.762699109494544e-4
allele num: 15946
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 5.405e0

QD
type: SiteQuality
SIO_000300: 8.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.532837e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.082e0

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

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512035805007863e-5
allele num: 66136
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.631578947368421e-4
allele num: 11400
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: 876
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.082e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

DP
type: SiteQuality
SIO_000300: 1.532837e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 5.405e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 813
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3175
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 3693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.264287655103704e-4
allele num: 66246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.520218911523259e-4
allele num: 6578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

DP
type: SiteQuality
SIO_000300: 1.536647e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.2e1

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

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3178
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3738
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.555555555555556e-4
allele num: 16200
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.052385406922357e-3
allele num: 8552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 2.62e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

DP
type: SiteQuality
SIO_000300: 1.541994e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3765
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 443
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 3416
bin: 9.75e1
variant carriers: 294

GenotypeQuality
all individuals: 342
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

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

Latino
type: Population
allele count: 10
allele frequency: 8.703220191470844e-4
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 296
allele frequency: 3.034030340303403e-2
allele num: 9756
num of homozygotes: 12

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.55995e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

QD
type: SiteQuality
SIO_000300: 1.372e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.25e-2

GenotypeQuality
all individuals: 270
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 834
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GenotypeQuality
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GenotypeQuality
all individuals: 50095
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.002801120448179e-4
allele num: 8568
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.119e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

QD
type: SiteQuality
SIO_000300: 1.057e1

DP
type: SiteQuality
SIO_000300: 1.549259e6

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 835
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GenotypeQuality
all individuals: 866
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GenotypeQuality
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GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004897983713453e-5
allele num: 66558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.548919e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.259e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 9.369999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.743375174337517e-4
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.944e0

QD
type: SiteQuality
SIO_000300: 9.16e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e-1

DP
type: SiteQuality
SIO_000300: 1.548771e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.39e-1