2-152410532-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410532
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410532
    reference: chr 2
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
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.14333A>G
  hgvsp: ENSP00000172853.10:p.Tyr4778Cys
  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.14333A>G
  hgvsp: ENSP00000386259.1:p.Tyr4778Cys
  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.19436A>G
  hgvsp: ENSP00000474498.1:p.Tyr6479Cys
  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.19436A>G
  hgvsp: ENSP00000380505.3:p.Tyr6479Cys
  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.19436A>G
  hgvsp: ENSP00000473894.1:p.Tyr6479Cys
  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.19436A>G
  hgvsp: ENSP00000416578.2:p.Tyr6479Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3626A>G
  hgvsp: ENSP00000410961.1:p.Tyr1209Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7957
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3496
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3518
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr6479Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

2-152410535-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410535
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410535
    reference: chr 2
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
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.14330T>A
  hgvsp: ENSP00000172853.10:p.Leu4777Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3623T>A
  hgvsp: ENSP00000410961.1:p.Leu1208Gln
  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.19433T>A
  hgvsp: ENSP00000416578.2:p.Leu6478Gln
  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.14330T>A
  hgvsp: ENSP00000386259.1:p.Leu4777Gln
  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.19433T>A
  hgvsp: ENSP00000380505.3:p.Leu6478Gln
  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.19433T>A
  hgvsp: ENSP00000474498.1:p.Leu6478Gln
  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.19433T>A
  hgvsp: ENSP00000473894.1:p.Leu6478Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3494
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu6478Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS

2-152410538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410538
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410538
    reference: chr 2
allele count: 5
allele frequency: 4.143669302040343e-5
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14327G>A
  hgvsp: ENSP00000172853.10:p.Arg4776His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19430G>A
  hgvsp: ENSP00000380505.3:p.Arg6477His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19430G>A
  hgvsp: ENSP00000474498.1:p.Arg6477His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19430G>A
  hgvsp: ENSP00000473894.1:p.Arg6477His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14327G>A
  hgvsp: ENSP00000386259.1:p.Arg4776His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19430G>A
  hgvsp: ENSP00000416578.2:p.Arg6477His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3620G>A
  hgvsp: ENSP00000410961.1:p.Arg1207His
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3524
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Arg6477His
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

2-152410539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410539
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410539
    reference: chr 2
allele count: 2
allele frequency: 1.657440249279014e-5
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19429C>T
  hgvsp: ENSP00000416578.2:p.Arg6477Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619C>T
  hgvsp: ENSP00000410961.1:p.Arg1207Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19429C>T
  hgvsp: ENSP00000380505.3:p.Arg6477Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19429C>T
  hgvsp: ENSP00000473894.1:p.Arg6477Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19429C>T
  hgvsp: ENSP00000474498.1:p.Arg6477Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14326C>T
  hgvsp: ENSP00000172853.10:p.Arg4776Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14326C>T
  hgvsp: ENSP00000386259.1:p.Arg4776Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3526
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7948
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg6477Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

2-152410539-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410539
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410539
    reference: chr 2
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14326C>G
  hgvsp: ENSP00000386259.1:p.Arg4776Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19429C>G
  hgvsp: ENSP00000416578.2:p.Arg6477Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19429C>G
  hgvsp: ENSP00000474498.1:p.Arg6477Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14326C>G
  hgvsp: ENSP00000172853.10:p.Arg4776Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19429C>G
  hgvsp: ENSP00000473894.1:p.Arg6477Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19429C>G
  hgvsp: ENSP00000380505.3:p.Arg6477Gly
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619C>G
  hgvsp: ENSP00000410961.1:p.Arg1207Gly
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg6477Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-152410544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410544
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410544
    reference: chr 2
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19429-5T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19429-5T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-5T>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.19429-5T>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.19429-5T>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.14326-5T>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.14326-5T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3492
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: c.19429-5T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/2-152410545-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410545
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410545
    reference: chr 2
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19429-6T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19429-6T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19429-6T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14326-6T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19429-6T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14326-6T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-6T>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
hgvs: c.19429-6T>G
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

2-152410546-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410546
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410546
    reference: chr 2
allele count: 11
allele frequency: 9.118037135278514e-5
allele num: 120640
alternate allele: G
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.14326-7T>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.19429-7T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19429-7T>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.14326-7T>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.19429-7T>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.19429-7T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-7T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3536
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3491
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: c.19429-7T>C
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-152410556-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410556
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410556
    reference: chr 2
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-17T>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.14326-17T>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.19429-17T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19429-17T>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.14326-17T>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.19429-17T>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.19429-17T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37495
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

2-152410558-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410558
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410558
    reference: chr 2
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14326-19T>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.19429-19T>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.19429-19T>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.14326-19T>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.19429-19T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19429-19T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-19T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7878
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-152410559-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410559
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410559
    reference: chr 2
allele count: 13
allele frequency: 1.078033004395058e-4
allele num: 120590
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.14326-20A>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.19429-20A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-20A>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.19429-20A>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.19429-20A>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.19429-20A>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.14326-20A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

2-152410567-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410567
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410567
    reference: chr 2
allele count: 4
allele frequency: 3.317739955542284e-5
allele num: 120564
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.19429-28T>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.14326-28T>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.19429-28T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-28T>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.19429-28T>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.19429-28T>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.14326-28T>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7822
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3539
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

2-152410570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152410570
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152410570
    reference: chr 2
allele count: 25
allele frequency: 2.074516637623434e-4
allele num: 120510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19429-31G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3619-31G>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.14326-31G>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.19429-31G>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.14326-31G>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.19429-31G>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.19429-31G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7782
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36279
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

2-152411395-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411395
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411395
    reference: chr 2
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19428+50G>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.19428+50G>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.19428+50G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+50G>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.14325+50G>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.19428+50G>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.14325+50G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6613
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3186
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30697
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

2-152411400-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411400
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411400
    reference: chr 2
allele count: 1
allele frequency: 8.306613725848521e-6
allele num: 120386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19428+45G>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.14325+45G>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.14325+45G>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.19428+45G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19428+45G>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.19428+45G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+45G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9943
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6603
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

2-152411412-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411412
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411412
    reference: chr 2
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
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.19428+33G>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.14325+33G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+33G>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.19428+33G>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.14325+33G>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.19428+33G>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.19428+33G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33621
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-152411412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411412
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411412
    reference: chr 2
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19428+33G>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.19428+33G>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.19428+33G>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.19428+33G>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.14325+33G>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.14325+33G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+33G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6592
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33621
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-152411423-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411423
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411423
    reference: chr 2
allele count: 1
allele frequency: 8.297240337863626e-6
allele num: 120522
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.14325+22T>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.19428+22T>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.19428+22T>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.14325+22T>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+22T>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.19428+22T>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.19428+22T>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34074
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-152411428-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411428
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411428
    reference: chr 2
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+17G>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.14325+17G>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.19428+17G>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.19428+17G>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.19428+17G>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.14325+17G>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.19428+17G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6585
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34126
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

2-152411431-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411431
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411431
    reference: chr 2
allele count: 4
allele frequency: 3.317134659081486e-5
allele num: 120586
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.19428+14T>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.14325+14T>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.19428+14T>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.19428+14T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+14T>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.14325+14T>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.19428+14T>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14410
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34207
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-152411436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411436
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411436
    reference: chr 2
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19428+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19428+9G>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.19428+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19428+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14325+9G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14325+9G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

2-152411437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411437
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411437
    reference: chr 2
allele count: 5
allele frequency: 4.145524491758697e-5
allele num: 120612
alternate allele: A
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.19428+8C>T
  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.19428+8C>T
  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.19428+8C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+8C>T
  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.14325+8C>T
  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.14325+8C>T
  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.19428+8C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 7.25e1
  variant carriers: 0
hgvs: c.19428+8C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-152411440-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411440
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411440
    reference: chr 2
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+5G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19428+5G>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.19428+5G>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.19428+5G>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.19428+5G>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.14325+5G>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.14325+5G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6580
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34271
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
hgvs: c.19428+5G>C
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-152411444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411444
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411444
    reference: chr 2
allele count: 2
allele frequency: 1.657962364254331e-5
allele num: 120630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19428+1G>A
  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.14325+1G>A
  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.19428+1G>A
  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.19428+1G>A
  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.19428+1G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14325+1G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3618+1G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6580
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: c.19428+1G>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

2-152411447-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411447
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411447
    reference: chr 2
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19426G>A
  hgvsp: ENSP00000474498.1:p.Asp6476Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19426G>A
  hgvsp: ENSP00000380505.3:p.Asp6476Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3616G>A
  hgvsp: ENSP00000410961.1:p.Asp1206Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14323G>A
  hgvsp: ENSP00000172853.10:p.Asp4775Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19426G>A
  hgvsp: ENSP00000473894.1:p.Asp6476Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19426G>A
  hgvsp: ENSP00000416578.2:p.Asp6476Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14323G>A
  hgvsp: ENSP00000386259.1:p.Asp4775Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9975
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp6476Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

2-152411448-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411448
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411448
    reference: chr 2
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
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.19425C>T
  hgvsp: ENST00000427231.2:c.19425C>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.19425C>T
  hgvsp: ENST00000397345.3:c.19425C>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.19425C>T
  hgvsp: ENST00000604864.1:c.19425C>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.19425C>T
  hgvsp: ENST00000603639.1:c.19425C>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.14322C>T
  hgvsp: ENST00000409198.1:c.14322C>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.14322C>T
  hgvsp: ENST00000172853.10:c.14322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3615C>T
  hgvsp: ENST00000413693.1:c.3615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6578
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2972
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile6475Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

2-152411450-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411450
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411450
    reference: chr 2
allele count: 2
allele frequency: 1.657687525901368e-5
allele num: 120650
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.19423A>G
  hgvsp: ENSP00000474498.1:p.Ile6475Val
  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.19423A>G
  hgvsp: ENSP00000416578.2:p.Ile6475Val
  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.14320A>G
  hgvsp: ENSP00000386259.1:p.Ile4774Val
  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.14320A>G
  hgvsp: ENSP00000172853.10:p.Ile4774Val
  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.19423A>G
  hgvsp: ENSP00000380505.3:p.Ile6475Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3613A>G
  hgvsp: ENSP00000410961.1:p.Ile1205Val
  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.19423A>G
  hgvsp: ENSP00000473894.1:p.Ile6475Val
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6578
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile6475Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

2-152411455-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411455
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411455
    reference: chr 2
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19418T>C
  hgvsp: ENSP00000380505.3:p.Leu6473Pro
  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.19418T>C
  hgvsp: ENSP00000416578.2:p.Leu6473Pro
  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.14315T>C
  hgvsp: ENSP00000172853.10:p.Leu4772Pro
  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.19418T>C
  hgvsp: ENSP00000474498.1:p.Leu6473Pro
  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.19418T>C
  hgvsp: ENSP00000473894.1:p.Leu6473Pro
  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.14315T>C
  hgvsp: ENSP00000386259.1:p.Leu4772Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3608T>C
  hgvsp: ENSP00000410961.1:p.Leu1203Pro
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14424
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34312
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu6473Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/2-152411463-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411463
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411463
    reference: chr 2
allele count: 1
allele frequency: 8.287063893262618e-6
allele num: 120670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14307T>G
  hgvsp: ENST00000172853.10:c.14307T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19410T>G
  hgvsp: ENST00000427231.2:c.19410T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3600T>G
  hgvsp: ENST00000413693.1:c.3600T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14307T>G
  hgvsp: ENST00000409198.1:c.14307T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19410T>G
  hgvsp: ENST00000603639.1:c.19410T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19410T>G
  hgvsp: ENST00000604864.1:c.19410T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19410T>G
  hgvsp: ENST00000397345.3:c.19410T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6577
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9980
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val6470Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

2-152411467-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411467
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411467
    reference: chr 2
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
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.19406G>C
  hgvsp: ENSP00000380505.3:p.Arg6469Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3596G>C
  hgvsp: ENSP00000410961.1:p.Arg1199Pro
  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.14303G>C
  hgvsp: ENSP00000386259.1:p.Arg4768Pro
  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.19406G>C
  hgvsp: ENSP00000416578.2:p.Arg6469Pro
  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.19406G>C
  hgvsp: ENSP00000473894.1:p.Arg6469Pro
  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.14303G>C
  hgvsp: ENSP00000172853.10:p.Arg4768Pro
  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.19406G>C
  hgvsp: ENSP00000474498.1:p.Arg6469Pro
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9981
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg6469Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

2-152411467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411467
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411467
    reference: chr 2
allele count: 6
allele frequency: 4.972320747837041e-5
allele num: 120668
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.14303G>A
  hgvsp: ENSP00000386259.1:p.Arg4768Gln
  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.19406G>A
  hgvsp: ENSP00000473894.1:p.Arg6469Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3596G>A
  hgvsp: ENSP00000410961.1:p.Arg1199Gln
  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.14303G>A
  hgvsp: ENSP00000172853.10:p.Arg4768Gln
  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.19406G>A
  hgvsp: ENSP00000380505.3:p.Arg6469Gln
  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.19406G>A
  hgvsp: ENSP00000416578.2:p.Arg6469Gln
  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.19406G>A
  hgvsp: ENSP00000474498.1:p.Arg6469Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9981
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg6469Gln
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-152411471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411471
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411471
    reference: chr 2
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
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.14299C>T
  hgvsp: ENSP00000172853.10:p.Leu4767Phe
  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.19402C>T
  hgvsp: ENSP00000473894.1:p.Leu6468Phe
  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.14299C>T
  hgvsp: ENSP00000386259.1:p.Leu4767Phe
  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.19402C>T
  hgvsp: ENSP00000474498.1:p.Leu6468Phe
  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.19402C>T
  hgvsp: ENSP00000416578.2:p.Leu6468Phe
  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.19402C>T
  hgvsp: ENSP00000380505.3:p.Leu6468Phe
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3592C>T
  hgvsp: ENSP00000410961.1:p.Leu1198Phe
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34330
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu6468Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

2-152411472-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411472
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411472
    reference: chr 2
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
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.19401C>G
  hgvsp: ENSP00000416578.2:p.Cys6467Trp
  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.19401C>G
  hgvsp: ENSP00000474498.1:p.Cys6467Trp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3591C>G
  hgvsp: ENSP00000410961.1:p.Cys1197Trp
  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.14298C>G
  hgvsp: ENSP00000172853.10:p.Cys4766Trp
  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.19401C>G
  hgvsp: ENSP00000473894.1:p.Cys6467Trp
  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.19401C>G
  hgvsp: ENSP00000380505.3:p.Cys6467Trp
  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.14298C>G
  hgvsp: ENSP00000386259.1:p.Cys4766Trp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9982
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys6467Trp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

2-152411476-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411476
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411476
    reference: chr 2
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
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.19397G>C
  hgvsp: ENSP00000380505.3:p.Arg6466Pro
  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.14294G>C
  hgvsp: ENSP00000172853.10:p.Arg4765Pro
  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.19397G>C
  hgvsp: ENSP00000473894.1:p.Arg6466Pro
  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.14294G>C
  hgvsp: ENSP00000386259.1:p.Arg4765Pro
  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.19397G>C
  hgvsp: ENSP00000416578.2:p.Arg6466Pro
  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.19397G>C
  hgvsp: ENSP00000474498.1:p.Arg6466Pro
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3587G>C
  hgvsp: ENSP00000410961.1:p.Arg1196Pro
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9980
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg6466Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

2-152411476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411476
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411476
    reference: chr 2
allele count: 3
allele frequency: 2.48562480322137e-5
allele num: 120694
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.19397G>A
  hgvsp: ENSP00000416578.2:p.Arg6466Gln
  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.19397G>A
  hgvsp: ENSP00000380505.3:p.Arg6466Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3587G>A
  hgvsp: ENSP00000410961.1:p.Arg1196Gln
  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.19397G>A
  hgvsp: ENSP00000474498.1:p.Arg6466Gln
  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.14294G>A
  hgvsp: ENSP00000386259.1:p.Arg4765Gln
  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.14294G>A
  hgvsp: ENSP00000172853.10:p.Arg4765Gln
  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.19397G>A
  hgvsp: ENSP00000473894.1:p.Arg6466Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6573
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg6466Gln
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

2-152411477-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411477
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411477
    reference: chr 2
allele count: 6
allele frequency: 4.971167230065619e-5
allele num: 120696
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.14293C>T
  hgvsp: ENSP00000386259.1:p.Arg4765Trp
  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.19396C>T
  hgvsp: ENSP00000416578.2:p.Arg6466Trp
  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.14293C>T
  hgvsp: ENSP00000172853.10:p.Arg4765Trp
  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.19396C>T
  hgvsp: ENSP00000380505.3:p.Arg6466Trp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3586C>T
  hgvsp: ENSP00000410961.1:p.Arg1196Trp
  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.19396C>T
  hgvsp: ENSP00000474498.1:p.Arg6466Trp
  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.19396C>T
  hgvsp: ENSP00000473894.1:p.Arg6466Trp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6570
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg6466Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-152411484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411484
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411484
    reference: chr 2
allele count: 5
allele frequency: 4.142502071251036e-5
allele num: 120700
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.19389C>T
  hgvsp: ENST00000604864.1:c.19389C>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.19389C>T
  hgvsp: ENST00000427231.2:c.19389C>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.14286C>T
  hgvsp: ENST00000172853.10:c.14286C>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.19389C>T
  hgvsp: ENST00000397345.3:c.19389C>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.19389C>T
  hgvsp: ENST00000603639.1:c.19389C>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.14286C>T
  hgvsp: ENST00000409198.1:c.14286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3579C>T
  hgvsp: ENST00000413693.1:c.3579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6566
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn6463Asn
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

2-152411487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411487
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411487
    reference: chr 2
allele count: 2
allele frequency: 1.657055743355207e-5
allele num: 120696
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19386G>A
  hgvsp: ENST00000397345.3:c.19386G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3576G>A
  hgvsp: ENST00000413693.1:c.3576G>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.19386G>A
  hgvsp: ENST00000427231.2:c.19386G>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.14283G>A
  hgvsp: ENST00000172853.10:c.14283G>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.14283G>A
  hgvsp: ENST00000409198.1:c.14283G>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.19386G>A
  hgvsp: ENST00000603639.1:c.19386G>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.19386G>A
  hgvsp: ENST00000604864.1:c.19386G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9982
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro6462Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-152411488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411488
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411488
    reference: chr 2
allele count: 3
allele frequency: 2.48562480322137e-5
allele num: 120694
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.19385C>T
  hgvsp: ENSP00000416578.2:p.Pro6462Leu
  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.14282C>T
  hgvsp: ENSP00000386259.1:p.Pro4761Leu
  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.14282C>T
  hgvsp: ENSP00000172853.10:p.Pro4761Leu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3575C>T
  hgvsp: ENSP00000410961.1:p.Pro1192Leu
  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.19385C>T
  hgvsp: ENSP00000380505.3:p.Pro6462Leu
  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.19385C>T
  hgvsp: ENSP00000473894.1:p.Pro6462Leu
  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.19385C>T
  hgvsp: ENSP00000474498.1:p.Pro6462Leu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6560
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro6462Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

2-152411495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411495
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411495
    reference: chr 2
allele count: 15
allele frequency: 1.242771214104625e-4
allele num: 120698
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.19378G>A
  hgvsp: ENSP00000416578.2:p.Asp6460Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3568G>A
  hgvsp: ENSP00000410961.1:p.Asp1190Asn
  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.19378G>A
  hgvsp: ENSP00000473894.1:p.Asp6460Asn
  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.19378G>A
  hgvsp: ENSP00000380505.3:p.Asp6460Asn
  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.14275G>A
  hgvsp: ENSP00000172853.10:p.Asp4759Asn
  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.14275G>A
  hgvsp: ENSP00000386259.1:p.Asp4759Asn
  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.19378G>A
  hgvsp: ENSP00000474498.1:p.Asp6460Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp6460Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

2-152411496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411496
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411496
    reference: chr 2
allele count: 65
allele frequency: 5.385520406979634e-4
allele num: 120694
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.14274C>T
  hgvsp: ENST00000172853.10:c.14274C>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.14274C>T
  hgvsp: ENST00000409198.1:c.14274C>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.19377C>T
  hgvsp: ENST00000604864.1:c.19377C>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.19377C>T
  hgvsp: ENST00000397345.3:c.19377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3567C>T
  hgvsp: ENST00000413693.1:c.3567C>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.19377C>T
  hgvsp: ENST00000603639.1:c.19377C>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.19377C>T
  hgvsp: ENST00000427231.2:c.19377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 9.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6564
  bin: 9.75e1
  variant carriers: 65
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp6459Asp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

2-152411501-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411501
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411501
    reference: chr 2
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19372G>C
  hgvsp: ENSP00000416578.2:p.Val6458Leu
  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.19372G>C
  hgvsp: ENSP00000474498.1:p.Val6458Leu
  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.19372G>C
  hgvsp: ENSP00000473894.1:p.Val6458Leu
  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.19372G>C
  hgvsp: ENSP00000380505.3:p.Val6458Leu
  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.14269G>C
  hgvsp: ENSP00000386259.1:p.Val4757Leu
  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.14269G>C
  hgvsp: ENSP00000172853.10:p.Val4757Leu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3562G>C
  hgvsp: ENSP00000410961.1:p.Val1188Leu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34382
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val6458Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-152411502-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411502
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411502
    reference: chr 2
allele count: 5
allele frequency: 4.14270800536895e-5
allele num: 120694
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.14268T>G
  hgvsp: ENSP00000386259.1:p.Ser4756Arg
  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.19371T>G
  hgvsp: ENSP00000380505.3:p.Ser6457Arg
  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.19371T>G
  hgvsp: ENSP00000474498.1:p.Ser6457Arg
  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.19371T>G
  hgvsp: ENSP00000416578.2:p.Ser6457Arg
  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.19371T>G
  hgvsp: ENSP00000473894.1:p.Ser6457Arg
  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.14268T>G
  hgvsp: ENSP00000172853.10:p.Ser4756Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3561T>G
  hgvsp: ENSP00000410961.1:p.Ser1187Arg
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6510
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser6457Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-152411510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411510
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411510
    reference: chr 2
allele count: 4
allele frequency: 3.314331167970303e-5
allele num: 120688
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.14260C>T
  hgvsp: ENSP00000386259.1:p.Pro4754Ser
  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.19363C>T
  hgvsp: ENSP00000473894.1:p.Pro6455Ser
  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.19363C>T
  hgvsp: ENSP00000380505.3:p.Pro6455Ser
  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.19363C>T
  hgvsp: ENSP00000474498.1:p.Pro6455Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3553C>T
  hgvsp: ENSP00000410961.1:p.Pro1185Ser
  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.14260C>T
  hgvsp: ENSP00000172853.10:p.Pro4754Ser
  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.19363C>T
  hgvsp: ENSP00000416578.2:p.Pro6455Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6505
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro6455Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

2-152411515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411515
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411515
    reference: chr 2
allele count: 7
allele frequency: 5.800560168381975e-5
allele num: 120678
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.14255C>T
  hgvsp: ENSP00000172853.10:p.Thr4752Met
  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.19358C>T
  hgvsp: ENSP00000473894.1:p.Thr6453Met
  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.14255C>T
  hgvsp: ENSP00000386259.1:p.Thr4752Met
  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.19358C>T
  hgvsp: ENSP00000380505.3:p.Thr6453Met
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3548C>T
  hgvsp: ENSP00000410961.1:p.Thr1183Met
  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.19358C>T
  hgvsp: ENSP00000416578.2:p.Thr6453Met
  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.19358C>T
  hgvsp: ENSP00000474498.1:p.Thr6453Met
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6505
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr6453Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

2-152411517-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411517
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411517
    reference: chr 2
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3546T>C
  hgvsp: ENST00000413693.1:c.3546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19356T>C
  hgvsp: ENST00000397345.3:c.19356T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14253T>C
  hgvsp: ENST00000409198.1:c.14253T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19356T>C
  hgvsp: ENST00000604864.1:c.19356T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19356T>C
  hgvsp: ENST00000427231.2:c.19356T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14253T>C
  hgvsp: ENST00000172853.10:c.14253T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19356T>C
  hgvsp: ENST00000603639.1:c.19356T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6500
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34367
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr6452Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

2-152411524-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411524
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411524
    reference: chr 2
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
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.14246C>T
  hgvsp: ENSP00000172853.10:p.Ala4749Val
  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.19349C>T
  hgvsp: ENSP00000380505.3:p.Ala6450Val
  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.19349C>T
  hgvsp: ENSP00000416578.2:p.Ala6450Val
  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.14246C>T
  hgvsp: ENSP00000386259.1:p.Ala4749Val
  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.19349C>T
  hgvsp: ENSP00000474498.1:p.Ala6450Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3539C>T
  hgvsp: ENSP00000410961.1:p.Ala1180Val
  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.19349C>T
  hgvsp: ENSP00000473894.1:p.Ala6450Val
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6500
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala6450Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-152411547-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411547
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411547
    reference: chr 2
allele count: 20
allele frequency: 1.658952537367906e-4
allele num: 120558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3516G>C
  hgvsp: ENST00000413693.1:c.3516G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19326G>C
  hgvsp: ENST00000427231.2:c.19326G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19326G>C
  hgvsp: ENST00000397345.3:c.19326G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14223G>C
  hgvsp: ENST00000172853.10:c.14223G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19326G>C
  hgvsp: ENST00000603639.1:c.19326G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19326G>C
  hgvsp: ENST00000604864.1:c.19326G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14223G>C
  hgvsp: ENST00000409198.1:c.14223G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6506
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9973
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34217
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg6442Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-152411548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411548
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411548
    reference: chr 2
allele count: 10
allele frequency: 8.296138976920142e-5
allele num: 120538
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.19325G>A
  hgvsp: ENSP00000474498.1:p.Arg6442Gln
  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.19325G>A
  hgvsp: ENSP00000380505.3:p.Arg6442Gln
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3515G>A
  hgvsp: ENSP00000410961.1:p.Arg1172Gln
  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.19325G>A
  hgvsp: ENSP00000473894.1:p.Arg6442Gln
  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.19325G>A
  hgvsp: ENSP00000416578.2:p.Arg6442Gln
  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.14222G>A
  hgvsp: ENSP00000172853.10:p.Arg4741Gln
  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.14222G>A
  hgvsp: ENSP00000386259.1:p.Arg4741Gln
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg6442Gln
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

2-152411549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411549
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411549
    reference: chr 2
allele count: 3
allele frequency: 2.489048187972919e-5
allele num: 120528
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.19324C>T
  hgvsp: ENSP00000416578.2:p.Arg6442Trp
  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.19324C>T
  hgvsp: ENSP00000380505.3:p.Arg6442Trp
  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.19324C>T
  hgvsp: ENSP00000473894.1:p.Arg6442Trp
  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.19324C>T
  hgvsp: ENSP00000474498.1:p.Arg6442Trp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3514C>T
  hgvsp: ENSP00000410961.1:p.Arg1172Trp
  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.14221C>T
  hgvsp: ENSP00000386259.1:p.Arg4741Trp
  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.14221C>T
  hgvsp: ENSP00000172853.10:p.Arg4741Trp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2534
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg6442Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-152411554-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411554
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411554
    reference: chr 2
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
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.19319A>G
  hgvsp: ENSP00000380505.3:p.Lys6440Arg
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3509A>G
  hgvsp: ENSP00000410961.1:p.Lys1170Arg
  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.19319A>G
  hgvsp: ENSP00000416578.2:p.Lys6440Arg
  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.19319A>G
  hgvsp: ENSP00000474498.1:p.Lys6440Arg
  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.14216A>G
  hgvsp: ENSP00000172853.10:p.Lys4739Arg
  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.14216A>G
  hgvsp: ENSP00000386259.1:p.Lys4739Arg
  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.19319A>G
  hgvsp: ENSP00000473894.1:p.Lys6440Arg
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys6440Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

2-152411556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411556
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411556
    reference: chr 2
allele count: 7
allele frequency: 5.815305885089556e-5
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14214C>T
  hgvsp: ENST00000172853.10:c.14214C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19317C>T
  hgvsp: ENST00000427231.2:c.19317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19317C>T
  hgvsp: ENST00000397345.3:c.19317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3507C>T
  hgvsp: ENST00000413693.1:c.3507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19317C>T
  hgvsp: ENST00000604864.1:c.19317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14214C>T
  hgvsp: ENST00000409198.1:c.14214C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19317C>T
  hgvsp: ENST00000603639.1:c.19317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14433
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
hgvs: c.19317C>T
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

2-152411556-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411556
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411556
    reference: chr 2
allele count: 1
allele frequency: 8.307579835842223e-6
allele num: 120372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14214C>A
  hgvsp: ENST00000172853.10:c.14214C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19317C>A
  hgvsp: ENST00000604864.1:c.19317C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3507C>A
  hgvsp: ENST00000413693.1:c.3507C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19317C>A
  hgvsp: ENST00000397345.3:c.19317C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19317C>A
  hgvsp: ENST00000427231.2:c.19317C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19317C>A
  hgvsp: ENST00000603639.1:c.19317C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14214C>A
  hgvsp: ENST00000409198.1:c.14214C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33941
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
hgvs: c.19317C>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-152411557-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411557
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411557
    reference: chr 2
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19316T>A
  hgvsp: ENSP00000473894.1:p.Ile6439Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14213T>A
  hgvsp: ENSP00000172853.10:p.Ile4738Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3506T>A
  hgvsp: ENSP00000410961.1:p.Ile1169Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19316T>A
  hgvsp: ENSP00000380505.3:p.Ile6439Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19316T>A
  hgvsp: ENSP00000416578.2:p.Ile6439Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14213T>A
  hgvsp: ENSP00000386259.1:p.Ile4738Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19316T>A
  hgvsp: ENSP00000474498.1:p.Ile6439Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33979
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9917
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile6439Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-152411561-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411561
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411561
    reference: chr 2
allele count: 1
allele frequency: 8.316008316008316e-6
allele num: 120250
alternate allele: T
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.19315-3T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19315-3T>A
  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.19315-3T>A
  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.19315-3T>A
  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.14212-3T>A
  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.14212-3T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3505-3T>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2518
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9884
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2964
  bin: 7.75e1
  variant carriers: 0
hgvs: c.19315-3T>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-152411562-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411562
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411562
    reference: chr 2
allele count: 11
allele frequency: 9.147913444106249e-5
allele num: 120246
alternate allele: C
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.19315-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14212-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19315-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19315-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3505-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19315-4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14212-4A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9882
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: c.19315-4A>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

2-152411563-AGAGAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411563
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411557
    reference: chr 2
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
alternate allele: A
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.19315-11_19315-6delATTCTC
  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.19315-11_19315-6delATTCTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19315-11_19315-6delATTCTC
  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.19315-11_19315-6delATTCTC
  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.14212-11_14212-6delATTCTC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3505-11_3505-6delATTCTC
  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.14212-11_14212-6delATTCTC
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2963
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33701
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
hgvs: c.19315-11_19315-6delATTCTC
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: AGAGAAT
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

2-152411568-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411568
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411568
    reference: chr 2
allele count: 21
allele frequency: 1.752482683802053e-4
allele num: 119830
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.19315-10T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3505-10T>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.14212-10T>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.14212-10T>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.19315-10T>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.19315-10T>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.19315-10T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  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: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2484
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-152411604-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152411604
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152411604
    reference: chr 2
allele count: 9
allele frequency: 7.766521116307968e-5
allele num: 115882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.19315-46C>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.19315-46C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3505-46C>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.14212-46C>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.19315-46C>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.19315-46C>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.14212-46C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11479
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10956
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6027
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

2-152417058-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417058
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417058
    reference: chr 2
allele count: 1
allele frequency: 3.115653040877368e-5
allele num: 32096
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.19314+48C>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.19314+48C>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.14211+48C>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.14211+48C>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.19314+48C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+48C>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.19314+48C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14287
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7186
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS

2-152417064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417064
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417064
    reference: chr 2
allele count: 12779
allele frequency: 3.630604011591568e-1
allele num: 35198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14211+42C>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.14211+42C>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.19314+42C>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.19314+42C>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.19314+42C>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.19314+42C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+42C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 1.25e1
  variant carriers: 4960
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 9.75e1
  variant carriers: 618
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 1.75e1
  variant carriers: 1333
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 2.75e1
  variant carriers: 357
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 2.25e1
  variant carriers: 493
genotype depth: GenotypeDepth
  all individuals: 23039
  bin: 7.5e0
  variant carriers: 10781
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 16271
  bin: 2.5e0
  variant carriers: 1732
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 323
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 367
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.25e1
  variant carriers: 274
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.75e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 3.25e1
  variant carriers: 279
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 385
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 6.75e1
  variant carriers: 615
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.75e1
  variant carriers: 389
genotype quality: GenotypeQuality
  all individuals: 4416
  bin: 1.75e1
  variant carriers: 1648
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 4.25e1
  variant carriers: 330
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 1.25e1
  variant carriers: 867
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 3.75e1
  variant carriers: 527
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.75e1
  variant carriers: 524
genotype quality: GenotypeQuality
  all individuals: 9239
  bin: 9.75e1
  variant carriers: 8669
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 6.25e1
  variant carriers: 773
genotype quality: GenotypeQuality
  all individuals: 5259
  bin: 2.5e0
  variant carriers: 121
num of homozygotes: 2373
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ

2-152417067-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417067
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417067
    reference: chr 2
allele count: 2
allele frequency: 5.395198273536552e-5
allele num: 37070
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.19314+39C>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.14211+39C>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+39C>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.19314+39C>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.14211+39C>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.19314+39C>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.19314+39C>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23408
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14182
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5508
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 13530
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4964
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

2-152417069-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417069
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417069
    reference: chr 2
allele count: 2
allele frequency: 5.302789267154523e-5
allele num: 37716
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19314+37C>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.14211+37C>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.19314+37C>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.14211+37C>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.19314+37C>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.19314+37C>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+37C>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24093
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16209
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4928
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13368
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4448
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2737
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.75e1
  variant carriers: 0
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: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

2-152417074-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417074
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417074
    reference: chr 2
allele count: 1
allele frequency: 2.593630044610437e-5
allele num: 38556
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.19314+32A>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.19314+32A>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.14211+32A>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.19314+32A>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.19314+32A>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.14211+32A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+32A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13186
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20420
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

2-152417081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417081
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417081
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 44164
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.19314+25C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+25C>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.19314+25C>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.14211+25C>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.19314+25C>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.19314+25C>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.14211+25C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29860
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3282
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

2-152417084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417084
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417084
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 46536
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.19314+22C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+22C>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.14211+22C>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.19314+22C>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.19314+22C>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.14211+22C>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.19314+22C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30832
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5405
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29598
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

2-152417089-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417089
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417089
    reference: chr 2
allele count: 2
allele frequency: 3.943684189770083e-5
allele num: 50714
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.19314+17C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+17C>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.19314+17C>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.19314+17C>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.14211+17C>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.14211+17C>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.19314+17C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3549
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

2-152417093-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417093
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417093
    reference: chr 2
allele count: 1
allele frequency: 1.850755108084098e-5
allele num: 54032
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.19314+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.14211+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19314+13A>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.19314+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.19314+13A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.14211+13A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-152417100-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417100
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417100
    reference: chr 2
allele count: 4
allele frequency: 6.37531478116732e-5
allele num: 62742
alternate allele: T
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.19314+6T>A
  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.14211+6T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3504+6T>A
  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.14211+6T>A
  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.19314+6T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19314+6T>A
  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.19314+6T>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16485
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26869
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
hgvs: c.19314+6T>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-152417109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417109
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417109
    reference: chr 2
allele count: 291
allele frequency: 3.789950769711651e-3
allele num: 76782
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.19311C>T
  hgvsp: ENST00000604864.1:c.19311C>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.19311C>T
  hgvsp: ENST00000397345.3:c.19311C>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.14208C>T
  hgvsp: ENST00000409198.1:c.14208C>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.19311C>T
  hgvsp: ENST00000427231.2:c.19311C>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.14208C>T
  hgvsp: ENST00000172853.10:c.14208C>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: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3501C>T
  hgvsp: ENST00000413693.1:c.3501C>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.19311C>T
  hgvsp: ENST00000603639.1:c.19311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5367
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 20934
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 1.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23804
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21058
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser6437Ser
num of homozygotes: 3
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-152417114-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417114
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417114
    reference: chr 2
allele count: 1
allele frequency: 1.1964298533177e-5
allele num: 83582
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.19306G>T
  hgvsp: ENSP00000380505.3:p.Ala6436Ser
  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.19306G>T
  hgvsp: ENSP00000473894.1:p.Ala6436Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3496G>T
  hgvsp: ENSP00000410961.1:p.Ala1166Ser
  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.19306G>T
  hgvsp: ENSP00000474498.1:p.Ala6436Ser
  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.14203G>T
  hgvsp: ENSP00000172853.10:p.Ala4735Ser
  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.14203G>T
  hgvsp: ENSP00000386259.1:p.Ala4735Ser
  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.19306G>T
  hgvsp: ENSP00000416578.2:p.Ala6436Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17909
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala6436Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-152417121-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152417121
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152417122
    reference: chr 2
allele count: 1
allele frequency: 1.094930471915033e-5
allele num: 91330
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.19298dupA
  hgvsp: ENSP00000473894.1:p.His6434AlafsTer13
  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.19298dupA
  hgvsp: ENSP00000380505.3:p.His6434AlafsTer13
  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.19298dupA
  hgvsp: ENSP00000474498.1:p.His6434AlafsTer13
  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.14195dupA
  hgvsp: ENSP00000172853.10:p.His4733AlafsTer13
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.3488dupA
  hgvsp: ENSP00000410961.1:p.His1164AlafsTer13
  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.19298dupA
  hgvsp: ENSP00000416578.2:p.His6434AlafsTer13
  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.14195dupA
  hgvsp: ENSP00000386259.1:p.His4733AlafsTer13
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His6434AlafsTer13
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 1127
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 38027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 66712
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e0

QD
type: SiteQuality
SIO_000300: 1.546e1

DP
type: SiteQuality
SIO_000300: 1.563141e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 2407
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 37993
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3519
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
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: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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: 8596
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.07e-1

MQ
type: SiteQuality
SIO_000300: 5.988e1

DP
type: SiteQuality
SIO_000300: 1.562926e6

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

FS
type: SiteQuality
SIO_000300: 3.648e0

GenotypeQuality
all individuals: 1127
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e-1

DP
type: SiteQuality
SIO_000300: 1.563184e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.11e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: -1.86e-1

FS
type: SiteQuality
SIO_000300: 5.611e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37949
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3494
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
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: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 2.531e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

QD
type: SiteQuality
SIO_000300: 1.257e1

DP
type: SiteQuality
SIO_000300: 1.562883e6

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 37949
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

FS
type: SiteQuality
SIO_000300: 2.531e0

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 1.562883e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7945
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3527
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
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: 8592
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: 16488
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: 5.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.343e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.56e-1

DP
type: SiteQuality
SIO_000300: 1.562064e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3527
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2768
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37858
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7943
bin: 6.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.686e0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.455e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.482e1

DP
type: SiteQuality
SIO_000300: 1.561723e6

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7939
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 11
allele frequency: 6.673137587964086e-4
allele num: 16484
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
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: -4.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.456e1

FS
type: SiteQuality
SIO_000300: 7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.561773e6

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

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

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3489
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 9.75e1
variant carriers: 1

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
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: 11558
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.413e1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 1.276e0

DP
type: SiteQuality
SIO_000300: 1.558341e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

VQSLOD
type: SiteQuality
SIO_000300: -2.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

GenotypeQuality
all individuals: 2759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
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: 11556
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 1.5566e6

MQRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-1

GenotypeQuality
all individuals: 7
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variant carriers: 0

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

GenotypeQuality
all individuals: 1128
bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 3542
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 186
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.041649652919559e-4
allele num: 9796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
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: 10
allele frequency: 1.499790029395885e-4
allele num: 66676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.064e0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.27e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

DP
type: SiteQuality
SIO_000300: 1.557294e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 967
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variant carriers: 0

GenotypeQuality
all individuals: 3484
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 4
allele frequency: 4.658746797111577e-4
allele num: 8586
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.589e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

DP
type: SiteQuality
SIO_000300: 1.551144e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 2743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 9.75e1
variant carriers: 25

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 24
allele frequency: 2.796550920531345e-3
allele num: 8582
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.591e0

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.550848e6

QD
type: SiteQuality
SIO_000300: 1.269e1

FS
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

GenotypeQuality
all individuals: 9952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 827
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2023
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variant carriers: 0

GenotypeQuality
all individuals: 2644
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.963639e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.507e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.25e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.028e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

GenotypeQuality
all individuals: 1960
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1259
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GenotypeQuality
all individuals: 812
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.077e0

FS
type: SiteQuality
SIO_000300: 7.389e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

QD
type: SiteQuality
SIO_000300: 1.578e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.243e0

VQSLOD
type: SiteQuality
SIO_000300: -3.237e-1

DP
type: SiteQuality
SIO_000300: 1.965572e6

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 1244
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6592
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.97354e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

QD
type: SiteQuality
SIO_000300: 1.244e1

FS
type: SiteQuality
SIO_000300: 5.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.236e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

DP
type: SiteQuality
SIO_000300: 1.97354e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.244e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.236e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.531e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.977746e6

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

FS
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SIO_000300: 8.138e0

ClippingRankSum
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SIO_000300: -5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

MQ
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SIO_000300: 5.892e1

BaseQRankSum
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SIO_000300: -2.807e0

DP
type: SiteQuality
SIO_000300: 1.978446e6

VQSLOD
type: SiteQuality
SIO_000300: -1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.217e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.99895036737142e-5
allele num: 66690
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.54e-1

DP
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.7e-3

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16506
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East Asian
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allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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SIO_000300: 1.24e0

DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.117e0

QD
type: SiteQuality
SIO_000300: 1.51e1

GenotypeQuality
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variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.169317118802619e-4
allele num: 8552
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 4.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.131e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 1.979715e6

QD
type: SiteQuality
SIO_000300: 1.182e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.42e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.397e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.979446e6

FS
type: SiteQuality
SIO_000300: 3.709e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998410842253606e-5
allele num: 66702
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
SIO_000300: 5.485e0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.979644e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.765e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 9808
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

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

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

South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

East Asian
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Other
type: Population
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African
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 896
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -1.97e0

FS
type: SiteQuality
SIO_000300: 2.337e0

DP
type: SiteQuality
SIO_000300: 1.979954e6

VQSLOD
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SIO_000300: -1.3e-1

BaseQRankSum
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SIO_000300: 8.529999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 1.772e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.314e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.333e1

DP
type: SiteQuality
SIO_000300: 1.980009e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.791e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
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SIO_000300: -1.579e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
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SIO_000300: 9.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.980846e6

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

African
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allele count: 5
allele frequency: 5.098919029165817e-4
allele num: 9806
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.980846e6

FS
type: SiteQuality
SIO_000300: 1.791e0

QD
type: SiteQuality
SIO_000300: 1.189e1

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.579e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.209e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 1.979945e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.434e0

FS
type: SiteQuality
SIO_000300: 2.232e0

QD
type: SiteQuality
SIO_000300: 1.103e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.979973e6

MQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

Latino
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allele num: 11556
num of homozygotes: 0

QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele frequency: 2.596053997923157e-4
allele num: 11556
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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
allele num: 66726
num of homozygotes: 0

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

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

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

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

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

Other
type: Population
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Latino
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele count: 6
allele frequency: 8.991727610598249e-5
allele num: 66728
num of homozygotes: 0

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

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

Other
type: Population
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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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 7.49288176232579e-5
allele num: 66730
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.039567611666327e-4
allele num: 9806
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-1

FS
type: SiteQuality
SIO_000300: 1.094e0

DP
type: SiteQuality
SIO_000300: 1.979865e6

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

QD
type: SiteQuality
SIO_000300: 1.368e1

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

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

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

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.019783805833163e-4
allele num: 9806
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.738e0

MQRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.286e1

DP
type: SiteQuality
SIO_000300: 1.979939e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 15

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9978
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.460806367883717e-4
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.118702834998981e-4
allele num: 9806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

DP
type: SiteQuality
SIO_000300: 1.980709e6

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.224e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 789
bin: 8.75e1
variant carriers: 0

African
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allele count: 50
allele frequency: 5.099959200326397e-3
allele num: 9804
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164686699277894e-4
allele num: 8586
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: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.874969711654955e-4
allele num: 16508
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.235e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

DP
type: SiteQuality
SIO_000300: 1.985061e6

VQSLOD
type: SiteQuality
SIO_000300: 4.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1896
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 9994
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variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
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: 11554
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

DP
type: SiteQuality
SIO_000300: 1.977589e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.246e1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 1.878e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.829e0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028834504482675e-4
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.24e-1

FS
type: SiteQuality
SIO_000300: 1.179e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.328e1

DP
type: SiteQuality
SIO_000300: 1.977688e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 11554
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: 8590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995024129972123e-5
allele num: 66722
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.977336e6

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.396e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 9992
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
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: 3
allele frequency: 4.496807266840543e-5
allele num: 66714
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: 11554
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.060599877576005e-4
allele num: 9802
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.977313e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.007e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 66714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.33e0

QD
type: SiteQuality
SIO_000300: 1.36e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.976855e6

GenotypeQuality
all individuals: 34356
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 4
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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: 790
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

African
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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: 11550
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.261e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.976649e6

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

European (Finnish)
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allele count: 19
allele frequency: 2.876173175900696e-3
allele num: 6606
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.482e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.064e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
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SIO_000300: 1.975831e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 10

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

Other
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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: 11530
num of homozygotes: 0

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

South Asian
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allele frequency: 3.029568589432865e-4
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.502100588164687e-5
allele num: 66648
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: 3.82e0

InbreedingCoeff
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SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-1

FS
type: SiteQuality
SIO_000300: 3.251e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 1.974991e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 7.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501665616278023e-5
allele num: 66642
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.86e-1

QD
type: SiteQuality
SIO_000300: 1.437e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.345e0

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.974375e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

FS
type: SiteQuality
SIO_000300: 6.079e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

QD
type: SiteQuality
SIO_000300: 1.956e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: -9.46e-1

DP
type: SiteQuality
SIO_000300: 1.972598e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.051935561433037e-4
allele num: 66544
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 8.23e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.970854e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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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: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
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Other
type: Population
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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MQ
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MQRankSum
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BaseQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8520
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

Other
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allele num: 894
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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allele frequency: 1.022076860179886e-4
allele num: 9784
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Latino
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QD
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.517450682852807e-4
allele num: 6590
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
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African
type: Population
allele count: 1
allele frequency: 1.022076860179886e-4
allele num: 9784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.203731567860367e-4
allele num: 66460
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.574e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 1.005e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.75e0

MQ
type: SiteQuality
SIO_000300: 5.99e1

DP
type: SiteQuality
SIO_000300: 1.967373e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

GenotypeQuality
all individuals: 6478
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

QD
type: SiteQuality
SIO_000300: 8.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.308e0

MQ
type: SiteQuality
SIO_000300: 5.129e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.965859e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.174e0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1883
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6482
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 9721
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.719916288803627e-5
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 2.049180327868853e-3
allele num: 9760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66224
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.954919e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.574e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

GenotypeQuality
all individuals: 3951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 574
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GenotypeQuality
all individuals: 427
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variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6455
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1646
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 761
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2562
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.384775808133472e-4
allele num: 9590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63680
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.647789e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.366e1

GenotypeQuality
all individuals: 296
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9827
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3779
bin: 2.5e0
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GenotypeQuality
all individuals: 3293
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8455
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1936
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.668711656441718e-4
allele num: 1304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15620
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.658e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
type: SiteQuality
SIO_000300: 7.0404e5

QD
type: SiteQuality
SIO_000300: 3.107e1

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 854
bin: 5.75e1
variant carriers: 839

GenotypeQuality
all individuals: 7523
bin: 2.25e1
variant carriers: 1786

GenotypeQuality
all individuals: 770
bin: 5.25e1
variant carriers: 736

GenotypeQuality
all individuals: 10959
bin: 7.5e0
variant carriers: 657

GenotypeQuality
all individuals: 1827
bin: 3.25e1
variant carriers: 1092

GenotypeQuality
all individuals: 666
bin: 7.25e1
variant carriers: 462

GenotypeQuality
all individuals: 720
bin: 8.25e1
variant carriers: 587

GenotypeQuality
all individuals: 1985
bin: 2.75e1
variant carriers: 1246

GenotypeQuality
all individuals: 804
bin: 8.75e1
variant carriers: 750

GenotypeQuality
all individuals: 763
bin: 9.25e1
variant carriers: 698

South Asian
type: Population
allele count: 1603
allele frequency: 1.942559379544353e-1
allele num: 8252
num of homozygotes: 174

European (Finnish)
type: Population
allele count: 842
allele frequency: 4.067632850241546e-1
allele num: 2070
num of homozygotes: 146

East Asian
type: Population
allele count: 912
allele frequency: 4.989059080962801e-1
allele num: 1828
num of homozygotes: 217

Other
type: Population
allele count: 118
allele frequency: 3.641975308641975e-1
allele num: 324
num of homozygotes: 23

African
type: Population
allele count: 1500
allele frequency: 4.261363636363636e-1
allele num: 3520
num of homozygotes: 310

Latino
type: Population
allele count: 1082
allele frequency: 6.147727272727272e-1
allele num: 1760
num of homozygotes: 310

European (Non-Finnish)
type: Population
allele count: 6722
allele frequency: 3.853473973859207e-1
allele num: 17444
num of homozygotes: 1193

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.16e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

QD
type: SiteQuality
SIO_000300: 2.234e1

DP
type: SiteQuality
SIO_000300: 7.59238e5

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3092
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2678
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variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 1

GenotypeQuality
all individuals: 365
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variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2046
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.081665765278529e-4
allele num: 18490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1942
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

QD
type: SiteQuality
SIO_000300: 1.916e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.84e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

DP
type: SiteQuality
SIO_000300: 7.33711e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

GenotypeQuality
all individuals: 1230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5246
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 179
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variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 17007
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variant carriers: 0

GenotypeQuality
all individuals: 168
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GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 272
bin: 8.25e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.055297593921486e-4
allele num: 18952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.43562e5

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.967e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.53e-1

QD
type: SiteQuality
SIO_000300: 1.661e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11626
bin: 7.5e0
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GenotypeQuality
all individuals: 3368
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 127
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GenotypeQuality
all individuals: 368
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.96031746031746e-4
allele num: 2016
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.073e0

QD
type: SiteQuality
SIO_000300: 8.24e0

VQSLOD
type: SiteQuality
SIO_000300: -6.343e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.83e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 7.77357e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

GenotypeQuality
all individuals: 3130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 9.75e1
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GenotypeQuality
all individuals: 27942
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7202
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GenotypeQuality
all individuals: 8123
bin: 6.25e1
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GenotypeQuality
all individuals: 140
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GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.067e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.694e-1

DP
type: SiteQuality
SIO_000300: 8.41629e5

QD
type: SiteQuality
SIO_000300: 7.15e0

FS
type: SiteQuality
SIO_000300: 3.522e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 2221
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 341
bin: 4.25e1
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GenotypeQuality
all individuals: 433
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GenotypeQuality
all individuals: 1535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
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GenotypeQuality
all individuals: 3110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9674
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24372
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 2.628e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.388e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
type: SiteQuality
SIO_000300: 8.74758e5

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12167
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.421150278293135e-5
allele num: 26950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3112
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.22645e5

QD
type: SiteQuality
SIO_000300: 1.253e1

GenotypeQuality
all individuals: 520
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29647
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5150
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.073883161512027e-4
allele num: 9312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3454
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.52e1

VQSLOD
type: SiteQuality
SIO_000300: -9.097e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.528e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.115e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

DP
type: SiteQuality
SIO_000300: 9.53857e5

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 500
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19128
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.172058134083451e-4
allele num: 34128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5754
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.951e0

QD
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.177e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.257e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.548e0

DP
type: SiteQuality
SIO_000300: 1.036049e6

GenotypeQuality
all individuals: 2487
bin: 9.75e1
variant carriers: 281

GenotypeQuality
all individuals: 423
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 332
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 26400
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2187
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 359
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.34543578196829e-5
allele num: 42636
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.644736842105263e-3
allele num: 608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4436
num of homozygotes: 0

Latino
type: Population
allele count: 27
allele frequency: 4.421880117916803e-3
allele num: 6106
num of homozygotes: 0

African
type: Population
allele count: 262
allele frequency: 3.86089006778662e-2
allele num: 6786
num of homozygotes: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.158301e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

FS
type: SiteQuality
SIO_000300: 1.528e0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

QD
type: SiteQuality
SIO_000300: 1.566e1

GenotypeQuality
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 664
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
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variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.136386942403008e-5
allele num: 46808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.799e1

VQSLOD
type: SiteQuality
SIO_000300: -2.319e0

MQRankSum
type: SiteQuality
SIO_000300: -1.114e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

DP
type: SiteQuality
SIO_000300: 1.210927e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1