2-152376273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376273
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376273
    reference: chr 2
allele count: 1
allele frequency: 8.311446524153063e-6
allele num: 120316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17386C>T
  hgvsp: ENSP00000172853.10:p.Arg5796Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.22489C>T
  hgvsp: ENSP00000474498.1:p.Arg7497Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.357C>T
  hgvsp: ENSP00000389074.1:p.Arg120Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6679C>T
  hgvsp: ENSP00000410961.1:p.Arg2227Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22489C>T
  hgvsp: ENSP00000380505.3:p.Arg7497Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.227C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.22489C>T
  hgvsp: ENSP00000416578.2:p.Arg7497Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.17386C>T
  hgvsp: ENSP00000386259.1:p.Arg5796Ter
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.22489C>T
  hgvsp: ENSP00000473894.1:p.Arg7497Ter
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg7497Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

2-152376277-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376277
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376277
    reference: chr 2
allele count: 4
allele frequency: 3.326458652118954e-5
allele num: 120248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.353A>G
  hgvsp: ENST00000434685.1:c.353A>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.22485A>G
  hgvsp: ENST00000397345.3:c.22485A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17382A>G
  hgvsp: ENST00000172853.10:c.17382A>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.22485A>G
  hgvsp: ENST00000604864.1:c.22485A>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.22485A>G
  hgvsp: ENST00000427231.2:c.22485A>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.22485A>G
  hgvsp: ENST00000603639.1:c.22485A>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.17382A>G
  hgvsp: ENST00000409198.1:c.17382A>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.6675A>G
  hgvsp: ENST00000413693.1:c.6675A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.223A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7559
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys7495Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/2-152376287-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376287
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376287
    reference: chr 2
allele count: 1
allele frequency: 8.351567589236499e-6
allele num: 119738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-5G>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.17377-5G>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.22480-5G>T
  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.22480-5G>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.22480-5G>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.6670-5G>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.22480-5G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.213G>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.17377-5G>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 2.25e1
  variant carriers: 0
hgvs: c.22480-5G>T
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

2-152376294-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376294
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376294
    reference: chr 2
allele count: 1
allele frequency: 8.374507997655138e-6
allele num: 119410
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.17377-12A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.206A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-12A>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.17377-12A>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.6670-12A>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.22480-12A>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.22480-12A>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.22480-12A>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.22480-12A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-152376302-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376302
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376302
    reference: chr 2
allele count: 3
allele frequency: 2.521856086079354e-5
allele num: 118960
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.22480-20A>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.22480-20A>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.22480-20A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.198A>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.17377-20A>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.17377-20A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-20A>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.6670-20A>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.22480-20A>T
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ

2-152376304-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376304
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376304
    reference: chr 2
allele count: 1
allele frequency: 8.409155888931868e-6
allele num: 118918
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.22480-22G>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.22480-22G>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.22480-22G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.196G>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.17377-22G>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.17377-22G>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.22480-22G>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.6670-22G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-22G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

2-152376304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376304
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376304
    reference: chr 2
allele count: 6
allele frequency: 5.045493533359121e-5
allele num: 118918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.196G>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.6670-22G>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.22480-22G>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.22480-22G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-22G>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.17377-22G>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.17377-22G>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.22480-22G>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.22480-22G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7431
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27827
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

2-152376306-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376306
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376306
    reference: chr 2
allele count: 12
allele frequency: 1.009200544968294e-4
allele num: 118906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-24T>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.22480-24T>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.17377-24T>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.22480-24T>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.22480-24T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.194T>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.17377-24T>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.22480-24T>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.6670-24T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17026
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9142
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

2-152376314-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376314
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376314
    reference: chr 2
allele count: 1
allele frequency: 8.437394532568342e-6
allele num: 118520
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22480-32G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.186G>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.22480-32G>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.6670-32G>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.17377-32G>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.22480-32G>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.22480-32G>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.17377-32G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-32G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23592
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9127
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

2-152376321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376321
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376321
    reference: chr 2
allele count: 1
allele frequency: 8.474719910506958e-6
allele num: 117998
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.22480-39A>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.6670-39A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-39A>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.22480-39A>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.17377-39A>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.22480-39A>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.17377-39A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.179A>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.22480-39A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12915
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5890
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

2-152376323-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376323
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376323
    reference: chr 2
allele count: 1
allele frequency: 8.481332586976066e-6
allele num: 117906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.177T>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.22480-41T>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.17377-41T>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.17377-41T>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-41T>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.6670-41T>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.22480-41T>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.22480-41T>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.22480-41T>A
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3764
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3655
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18249
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-152376328-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152376328
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152376328
    reference: chr 2
allele count: 3
allele frequency: 2.556542191467967e-5
allele num: 117346
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22480-46T>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.6670-46T>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.22480-46T>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.17377-46T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000183091
  ensembl transcript: ENST00000483418
  gene symbol: NEB
  hgvsc: ENST00000483418.1:n.172T>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.17377-46T>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.22480-46T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.348-46T>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.22480-46T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14493
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3548
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13671
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/2-152380775-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380775
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380775
    reference: chr 2
allele count: 1
allele frequency: 8.43397881384522e-6
allele num: 118568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.22479+50G>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.17376+50G>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.22479+50G>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.22479+50G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+50G>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.17376+50G>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.6669+50G>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.22479+50G>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

2-152380775-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380775
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380773
    reference: chr 2
allele count: 1
allele frequency: 8.43397881384522e-6
allele num: 118568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+48_347+49delAA
  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.6669+48_6669+49delAA
  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.22479+48_22479+49delAA
  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.17376+48_17376+49delAA
  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.22479+48_22479+49delAA
  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.22479+48_22479+49delAA
  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.17376+48_17376+49delAA
  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.22479+48_22479+49delAA
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11713
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: CTT
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

2-152380784-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380784
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380781
    reference: chr 2
allele count: 2
allele frequency: 1.681944327642755e-5
allele num: 118910
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.22479+38_22479+40delGAG
  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.6669+38_6669+40delGAG
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+38_347+40delGAG
  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.22479+38_22479+40delGAG
  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.17376+38_17376+40delGAG
  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.22479+38_22479+40delGAG
  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.22479+38_22479+40delGAG
  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.17376+38_17376+40delGAG
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12203
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: TCTC
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-152380788-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380788
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380788
    reference: chr 2
allele count: 1
allele frequency: 8.401384548173538e-6
allele num: 119028
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.22479+37G>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.22479+37G>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+37G>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.22479+37G>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.17376+37G>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.22479+37G>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.17376+37G>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.6669+37G>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3028
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

2-152380792-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380792
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380792
    reference: chr 2
allele count: 2
allele frequency: 1.675855943423103e-5
allele num: 119342
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.22479+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.17376+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.6669+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.22479+33G>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.22479+33G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+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.17376+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.22479+33G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

2-152380793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380793
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380793
    reference: chr 2
allele count: 1
allele frequency: 8.367360599772408e-6
allele num: 119512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17376+32T>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.22479+32T>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.22479+32T>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.17376+32T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+32T>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.22479+32T>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.6669+32T>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.22479+32T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

2-152380801-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380801
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380801
    reference: chr 2
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
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.17376+24G>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.22479+24G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+24G>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.22479+24G>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.22479+24G>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.6669+24G>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.17376+24G>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.22479+24G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35369
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-152380814-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380814
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380814
    reference: chr 2
allele count: 1
allele frequency: 8.29985724245543e-6
allele num: 120484
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.22479+11T>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.6669+11T>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.22479+11T>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.22479+11T>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.22479+11T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+11T>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.17376+11T>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.17376+11T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2732
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13189
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

2-152380817-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380817
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380816
    reference: chr 2
allele count: 2
allele frequency: 1.659420530350801e-5
allele num: 120524
alternate allele: T
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.17376+7delC
  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.22479+7delC
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+7delC
  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.22479+7delC
  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.22479+7delC
  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.22479+7delC
  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.17376+7delC
  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.6669+7delC
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2734
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13203
  bin: 6.75e1
  variant carriers: 0
hgvs: c.22479+7delC
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: TG
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-152380821-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380821
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380821
    reference: chr 2
allele count: 4
allele frequency: 3.31746479340488e-5
allele num: 120574
alternate allele: C
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.17376+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.6669+4A>G
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22479+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.22479+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.17376+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: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.347+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.22479+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.22479+4A>G
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
hgvs: c.22479+4A>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

2-152380831-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380831
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380831
    reference: chr 2
allele count: 2
allele frequency: 1.657934876318058e-5
allele num: 120632
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.22473C>T
  hgvsp: ENST00000427231.2:c.22473C>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.17370C>T
  hgvsp: ENST00000409198.1:c.17370C>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.22473C>T
  hgvsp: ENST00000397345.3:c.22473C>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.22473C>T
  hgvsp: ENST00000603639.1:c.22473C>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.22473C>T
  hgvsp: ENST00000604864.1:c.22473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.341C>T
  hgvsp: ENST00000434685.1:c.341C>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.17370C>T
  hgvsp: ENST00000172853.10:c.17370C>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.6663C>T
  hgvsp: ENST00000413693.1:c.6663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11718
  bin: 3.25e1
  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: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser7491Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

2-152380836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380836
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380836
    reference: chr 2
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.17365C>T
  hgvsp: ENST00000409198.1:c.17365C>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.22468C>T
  hgvsp: ENST00000427231.2:c.22468C>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.17365C>T
  hgvsp: ENST00000172853.10:c.17365C>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.6658C>T
  hgvsp: ENST00000413693.1:c.6658C>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.22468C>T
  hgvsp: ENST00000604864.1:c.22468C>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.22468C>T
  hgvsp: ENST00000397345.3:c.22468C>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.22468C>T
  hgvsp: ENST00000603639.1:c.22468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.336C>T
  hgvsp: ENST00000434685.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu7490Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

2-152380852-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380852
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380852
    reference: chr 2
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.22452C>G
  hgvsp: ENST00000427231.2:c.22452C>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.22452C>G
  hgvsp: ENST00000604864.1:c.22452C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.320C>G
  hgvsp: ENST00000434685.1:c.320C>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.22452C>G
  hgvsp: ENST00000603639.1:c.22452C>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.17349C>G
  hgvsp: ENST00000409198.1:c.17349C>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.6642C>G
  hgvsp: ENST00000413693.1:c.6642C>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.22452C>G
  hgvsp: ENST00000397345.3:c.22452C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17349C>G
  hgvsp: ENST00000172853.10:c.17349C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3139
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala7484Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

2-152380854-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380854
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380854
    reference: chr 2
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.318G>A
  hgvsp: ENSP00000389074.1:p.Ala107Thr
  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.6640G>A
  hgvsp: ENSP00000410961.1:p.Ala2214Thr
  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.22450G>A
  hgvsp: ENSP00000474498.1:p.Ala7484Thr
  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.22450G>A
  hgvsp: ENSP00000380505.3:p.Ala7484Thr
  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.17347G>A
  hgvsp: ENSP00000172853.10:p.Ala5783Thr
  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.22450G>A
  hgvsp: ENSP00000416578.2:p.Ala7484Thr
  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.17347G>A
  hgvsp: ENSP00000386259.1:p.Ala5783Thr
  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.22450G>A
  hgvsp: ENSP00000473894.1:p.Ala7484Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala7484Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

2-152380870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380870
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380870
    reference: chr 2
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22434C>T
  hgvsp: ENST00000397345.3:c.22434C>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.6624C>T
  hgvsp: ENST00000413693.1:c.6624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.302C>T
  hgvsp: ENST00000434685.1:c.302C>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.17331C>T
  hgvsp: ENST00000409198.1:c.17331C>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.22434C>T
  hgvsp: ENST00000604864.1:c.22434C>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.22434C>T
  hgvsp: ENST00000603639.1:c.22434C>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.17331C>T
  hgvsp: ENST00000172853.10:c.17331C>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.22434C>T
  hgvsp: ENST00000427231.2:c.22434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg7478Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-152380871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380871
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380871
    reference: chr 2
allele count: 3
allele frequency: 2.484718978283556e-5
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.301G>A
  hgvsp: ENSP00000389074.1:p.Arg101His
  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.22433G>A
  hgvsp: ENSP00000416578.2:p.Arg7478His
  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.22433G>A
  hgvsp: ENSP00000473894.1:p.Arg7478His
  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.22433G>A
  hgvsp: ENSP00000474498.1:p.Arg7478His
  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.17330G>A
  hgvsp: ENSP00000172853.10:p.Arg5777His
  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.6623G>A
  hgvsp: ENSP00000410961.1:p.Arg2208His
  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.17330G>A
  hgvsp: ENSP00000386259.1:p.Arg5777His
  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.22433G>A
  hgvsp: ENSP00000380505.3:p.Arg7478His
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg7478His
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

2-152380872-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380872
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380872
    reference: chr 2
allele count: 31
allele frequency: 2.567372832226326e-4
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.300C>T
  hgvsp: ENSP00000389074.1:p.Arg101Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6622C>T
  hgvsp: ENSP00000410961.1:p.Arg2208Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17329C>T
  hgvsp: ENSP00000172853.10:p.Arg5777Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.22432C>T
  hgvsp: ENSP00000416578.2:p.Arg7478Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.17329C>T
  hgvsp: ENSP00000386259.1:p.Arg5777Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.22432C>T
  hgvsp: ENSP00000474498.1:p.Arg7478Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.22432C>T
  hgvsp: ENSP00000473894.1:p.Arg7478Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22432C>T
  hgvsp: ENSP00000380505.3:p.Arg7478Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg7478Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-152380876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380876
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380876
    reference: chr 2
allele count: 7
allele frequency: 5.797197469109219e-5
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.22428C>T
  hgvsp: ENST00000427231.2:c.22428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22428C>T
  hgvsp: ENST00000397345.3:c.22428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.17325C>T
  hgvsp: ENST00000409198.1:c.17325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.296C>T
  hgvsp: ENST00000434685.1:c.296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.22428C>T
  hgvsp: ENST00000603639.1:c.22428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.22428C>T
  hgvsp: ENST00000604864.1:c.22428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17325C>T
  hgvsp: ENST00000172853.10:c.17325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6618C>T
  hgvsp: ENST00000413693.1:c.6618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13252
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu7476Leu
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

2-152380880-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380880
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380880
    reference: chr 2
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
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.22424T>C
  hgvsp: ENSP00000416578.2:p.Met7475Thr
  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.22424T>C
  hgvsp: ENSP00000380505.3:p.Met7475Thr
  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.17321T>C
  hgvsp: ENSP00000172853.10:p.Met5774Thr
  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.17321T>C
  hgvsp: ENSP00000386259.1:p.Met5774Thr
  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.22424T>C
  hgvsp: ENSP00000473894.1:p.Met7475Thr
  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.6614T>C
  hgvsp: ENSP00000410961.1:p.Met2205Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.292T>C
  hgvsp: ENSP00000389074.1:p.Met98Thr
  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.22424T>C
  hgvsp: ENSP00000474498.1:p.Met7475Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met7475Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-152380889-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380889
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380889
    reference: chr 2
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
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.22415G>A
  hgvsp: ENSP00000416578.2:p.Gly7472Asp
  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.22415G>A
  hgvsp: ENSP00000380505.3:p.Gly7472Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.283G>A
  hgvsp: ENSP00000389074.1:p.Gly95Asp
  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.22415G>A
  hgvsp: ENSP00000474498.1:p.Gly7472Asp
  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.17312G>A
  hgvsp: ENSP00000386259.1:p.Gly5771Asp
  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.17312G>A
  hgvsp: ENSP00000172853.10:p.Gly5771Asp
  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.6605G>A
  hgvsp: ENSP00000410961.1:p.Gly2202Asp
  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.22415G>A
  hgvsp: ENSP00000473894.1:p.Gly7472Asp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13259
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly7472Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-152380890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380890
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380890
    reference: chr 2
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
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.22414G>A
  hgvsp: ENSP00000416578.2:p.Gly7472Ser
  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.6604G>A
  hgvsp: ENSP00000410961.1:p.Gly2202Ser
  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.17311G>A
  hgvsp: ENSP00000172853.10:p.Gly5771Ser
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.282G>A
  hgvsp: ENSP00000389074.1:p.Gly95Ser
  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.17311G>A
  hgvsp: ENSP00000386259.1:p.Gly5771Ser
  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.22414G>A
  hgvsp: ENSP00000473894.1:p.Gly7472Ser
  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.22414G>A
  hgvsp: ENSP00000474498.1:p.Gly7472Ser
  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.22414G>A
  hgvsp: ENSP00000380505.3:p.Gly7472Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly7472Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum

2-152380898-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380898
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380898
    reference: chr 2
allele count: 3
allele frequency: 2.484266313348791e-5
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.274G>C
  hgvsp: ENSP00000389074.1:p.Gly92Ala
  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.22406G>C
  hgvsp: ENSP00000380505.3:p.Gly7469Ala
  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.22406G>C
  hgvsp: ENSP00000473894.1:p.Gly7469Ala
  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.22406G>C
  hgvsp: ENSP00000474498.1:p.Gly7469Ala
  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.17303G>C
  hgvsp: ENSP00000172853.10:p.Gly5768Ala
  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.17303G>C
  hgvsp: ENSP00000386259.1:p.Gly5768Ala
  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.22406G>C
  hgvsp: ENSP00000416578.2:p.Gly7469Ala
  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.6596G>C
  hgvsp: ENSP00000410961.1:p.Gly2199Ala
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13261
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly7469Ala
num of homozygotes: 1
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-152380898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380898
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380898
    reference: chr 2
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22406G>A
  hgvsp: ENSP00000380505.3:p.Gly7469Asp
  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.17303G>A
  hgvsp: ENSP00000386259.1:p.Gly5768Asp
  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.22406G>A
  hgvsp: ENSP00000416578.2:p.Gly7469Asp
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.274G>A
  hgvsp: ENSP00000389074.1:p.Gly92Asp
  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.22406G>A
  hgvsp: ENSP00000474498.1:p.Gly7469Asp
  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.22406G>A
  hgvsp: ENSP00000473894.1:p.Gly7469Asp
  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.6596G>A
  hgvsp: ENSP00000410961.1:p.Gly2199Asp
  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.17303G>A
  hgvsp: ENSP00000172853.10:p.Gly5768Asp
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13261
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly7469Asp
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-152380900-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380900
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380900
    reference: chr 2
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.17301A>G
  hgvsp: ENST00000409198.1:c.17301A>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.6594A>G
  hgvsp: ENST00000413693.1:c.6594A>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.22404A>G
  hgvsp: ENST00000427231.2:c.22404A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.272A>G
  hgvsp: ENST00000434685.1:c.272A>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.22404A>G
  hgvsp: ENST00000604864.1:c.22404A>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.22404A>G
  hgvsp: ENST00000397345.3:c.22404A>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.22404A>G
  hgvsp: ENST00000603639.1:c.22404A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17301A>G
  hgvsp: ENST00000172853.10:c.17301A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu7468Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP

2-152380901-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380901
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380901
    reference: chr 2
allele count: 3
allele frequency: 2.484266313348791e-5
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.271A>C
  hgvsp: ENSP00000389074.1:p.Glu91Ala
  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.22403A>C
  hgvsp: ENSP00000473894.1:p.Glu7468Ala
  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.22403A>C
  hgvsp: ENSP00000474498.1:p.Glu7468Ala
  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.22403A>C
  hgvsp: ENSP00000416578.2:p.Glu7468Ala
  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.17300A>C
  hgvsp: ENSP00000172853.10:p.Glu5767Ala
  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.17300A>C
  hgvsp: ENSP00000386259.1:p.Glu5767Ala
  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.22403A>C
  hgvsp: ENSP00000380505.3:p.Glu7468Ala
  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.6593A>C
  hgvsp: ENSP00000410961.1:p.Glu2198Ala
  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: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu7468Ala
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

2-152380907-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380907
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380907
    reference: chr 2
allele count: 6
allele frequency: 4.968532626697582e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6587G>A
  hgvsp: ENSP00000410961.1:p.Arg2196His
  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.22397G>A
  hgvsp: ENSP00000380505.3:p.Arg7466His
  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.22397G>A
  hgvsp: ENSP00000473894.1:p.Arg7466His
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.265G>A
  hgvsp: ENSP00000389074.1:p.Arg89His
  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.22397G>A
  hgvsp: ENSP00000416578.2:p.Arg7466His
  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.17294G>A
  hgvsp: ENSP00000172853.10:p.Arg5765His
  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.22397G>A
  hgvsp: ENSP00000474498.1:p.Arg7466His
  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.17294G>A
  hgvsp: ENSP00000386259.1:p.Arg5765His
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg7466His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

2-152380908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380908
    reference: chr 2
allele count: 7
allele frequency: 5.796621397813846e-5
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.22396C>T
  hgvsp: ENSP00000473894.1:p.Arg7466Cys
  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.22396C>T
  hgvsp: ENSP00000416578.2:p.Arg7466Cys
  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.22396C>T
  hgvsp: ENSP00000380505.3:p.Arg7466Cys
  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.17293C>T
  hgvsp: ENSP00000172853.10:p.Arg5765Cys
  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.6586C>T
  hgvsp: ENSP00000410961.1:p.Arg2196Cys
  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.22396C>T
  hgvsp: ENSP00000474498.1:p.Arg7466Cys
  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.17293C>T
  hgvsp: ENSP00000386259.1:p.Arg5765Cys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.264C>T
  hgvsp: ENSP00000389074.1:p.Arg89Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg7466Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-152380912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380912
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380912
    reference: chr 2
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000416578
  ensembl transcript: ENST00000427231
  gene symbol: NEB
  hgvsc: ENST00000427231.2:c.22392G>A
  hgvsp: ENST00000427231.2:c.22392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22392G>A
  hgvsp: ENST00000397345.3:c.22392G>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.22392G>A
  hgvsp: ENST00000603639.1:c.22392G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.260G>A
  hgvsp: ENST00000434685.1:c.260G>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.17289G>A
  hgvsp: ENST00000409198.1:c.17289G>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.17289G>A
  hgvsp: ENST00000172853.10:c.17289G>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.22392G>A
  hgvsp: ENST00000604864.1:c.22392G>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.6582G>A
  hgvsp: ENST00000413693.1:c.6582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys7464Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

2-152380915-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380915
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380915
    reference: chr 2
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6579C>T
  hgvsp: ENST00000413693.1:c.6579C>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.17286C>T
  hgvsp: ENST00000172853.10:c.17286C>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.22389C>T
  hgvsp: ENST00000427231.2:c.22389C>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.22389C>T
  hgvsp: ENST00000604864.1:c.22389C>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.22389C>T
  hgvsp: ENST00000397345.3:c.22389C>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.22389C>T
  hgvsp: ENST00000603639.1:c.22389C>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.17286C>T
  hgvsp: ENST00000409198.1:c.17286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.257C>T
  hgvsp: ENST00000434685.1:c.257C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala7463Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

2-152380921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380921
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380921
    reference: chr 2
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17280C>T
  hgvsp: ENST00000172853.10:c.17280C>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.22383C>T
  hgvsp: ENST00000427231.2:c.22383C>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.22383C>T
  hgvsp: ENST00000603639.1:c.22383C>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.6573C>T
  hgvsp: ENST00000413693.1:c.6573C>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.22383C>T
  hgvsp: ENST00000397345.3:c.22383C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.251C>T
  hgvsp: ENST00000434685.1:c.251C>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.22383C>T
  hgvsp: ENST00000604864.1:c.22383C>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.17280C>T
  hgvsp: ENST00000409198.1:c.17280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36401
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13274
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr7461Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

2-152380922-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380922
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380922
    reference: chr 2
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.250A>G
  hgvsp: ENSP00000389074.1:p.Tyr84Cys
  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.22382A>G
  hgvsp: ENSP00000380505.3:p.Tyr7461Cys
  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.17279A>G
  hgvsp: ENSP00000386259.1:p.Tyr5760Cys
  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.6572A>G
  hgvsp: ENSP00000410961.1:p.Tyr2191Cys
  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.22382A>G
  hgvsp: ENSP00000474498.1:p.Tyr7461Cys
  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.17279A>G
  hgvsp: ENSP00000172853.10:p.Tyr5760Cys
  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.22382A>G
  hgvsp: ENSP00000473894.1:p.Tyr7461Cys
  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.22382A>G
  hgvsp: ENSP00000416578.2:p.Tyr7461Cys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr7461Cys
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-152380950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380950
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380950
    reference: chr 2
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17272-21T>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.22375-21T>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.6565-21T>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.22375-21T>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.17272-21T>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.22375-21T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.243-21T>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.22375-21T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

2-152380962-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380962
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380962
    reference: chr 2
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17272-33A>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.22375-33A>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.22375-33A>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.22375-33A>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.17272-33A>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.243-33A>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.6565-33A>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.22375-33A>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2719
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-152380963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380963
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380963
    reference: chr 2
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.243-34C>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.22375-34C>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.17272-34C>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.22375-34C>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.6565-34C>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.22375-34C>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.17272-34C>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.22375-34C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

2-152380994-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380994
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380994
    reference: chr 2
allele count: 4
allele frequency: 3.312519668085529e-5
allele num: 120754
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.6564+35C>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.22374+35C>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+35C>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.22374+35C>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.22374+35C>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.17271+35C>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.22374+35C>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.17271+35C>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14007
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3144
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-152380995-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380995
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380995
    reference: chr 2
allele count: 79
allele frequency: 6.571613955113382e-4
allele num: 120214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17271+34A>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.22374+34A>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.17271+34A>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.22374+34A>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.22374+34A>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+34A>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.22374+34A>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.6564+34A>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 9.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 9.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 13214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36277
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 9.25e1
  variant carriers: 3
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-152380999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152380999
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152380999
    reference: chr 2
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
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.22374+30C>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.17271+30C>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.6564+30C>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.22374+30C>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.22374+30C>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.17271+30C>T
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+30C>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.22374+30C>T
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13369
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

2-152381001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381001
    reference: chr 2
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
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.6564+28T>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.22374+28T>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.22374+28T>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+28T>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.22374+28T>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.17271+28T>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.22374+28T>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.17271+28T>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36488
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13371
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

2-152381009-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381009
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381009
    reference: chr 2
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
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.22374+20G>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.6564+20G>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.22374+20G>C
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+20G>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.22374+20G>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.17271+20G>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.17271+20G>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.22374+20G>C
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13366
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-152381022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381022
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381022
    reference: chr 2
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: T
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.17271+7G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+7G>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.22374+7G>A
  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.22374+7G>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.22374+7G>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.22374+7G>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.6564+7G>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.17271+7G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13366
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36509
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 9.25e1
  variant carriers: 0
hgvs: c.22374+7G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

2-152381023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381023
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381023
    reference: chr 2
allele count: 3
allele frequency: 2.484472049689441e-5
allele num: 120750
alternate allele: T
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.22374+6G>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.17271+6G>A
  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.22374+6G>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.22374+6G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+6G>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.22374+6G>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.17271+6G>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.6564+6G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13367
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
hgvs: c.22374+6G>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-152381024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381024
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381024
    reference: chr 2
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: T
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.22374+5G>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.17271+5G>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.22374+5G>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.22374+5G>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.6564+5G>A
  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.22374+5G>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.17271+5G>A
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.242+5G>A
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13903
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: c.22374+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

2-152381033-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381033
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381033
    reference: chr 2
allele count: 44
allele frequency: 3.643711285567591e-4
allele num: 120756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6560G>C
  hgvsp: ENSP00000410961.1:p.Ser2187Thr
  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.17267G>C
  hgvsp: ENSP00000386259.1:p.Ser5756Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.238G>C
  hgvsp: ENSP00000389074.1:p.Ser80Thr
  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.17267G>C
  hgvsp: ENSP00000172853.10:p.Ser5756Thr
  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.22370G>C
  hgvsp: ENSP00000474498.1:p.Ser7457Thr
  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.22370G>C
  hgvsp: ENSP00000416578.2:p.Ser7457Thr
  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.22370G>C
  hgvsp: ENSP00000473894.1:p.Ser7457Thr
  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.22370G>C
  hgvsp: ENSP00000380505.3:p.Ser7457Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser7457Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-152381043-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381043
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381043
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6550A>G
  hgvsp: ENSP00000410961.1:p.Lys2184Glu
  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.22360A>G
  hgvsp: ENSP00000474498.1:p.Lys7454Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.228A>G
  hgvsp: ENSP00000389074.1:p.Lys77Glu
  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.22360A>G
  hgvsp: ENSP00000416578.2:p.Lys7454Glu
  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.17257A>G
  hgvsp: ENSP00000386259.1:p.Lys5753Glu
  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.22360A>G
  hgvsp: ENSP00000473894.1:p.Lys7454Glu
  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.17257A>G
  hgvsp: ENSP00000172853.10:p.Lys5753Glu
  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.22360A>G
  hgvsp: ENSP00000380505.3:p.Lys7454Glu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
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: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys7454Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

2-152381054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381054
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381054
    reference: chr 2
allele count: 9
allele frequency: 7.452428663696736e-5
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000474498
  ensembl transcript: ENST00000604864
  gene symbol: NEB
  hgvsc: ENST00000604864.1:c.22349C>T
  hgvsp: ENSP00000474498.1:p.Thr7450Ile
  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.17246C>T
  hgvsp: ENSP00000386259.1:p.Thr5749Ile
  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.17246C>T
  hgvsp: ENSP00000172853.10:p.Thr5749Ile
  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.22349C>T
  hgvsp: ENSP00000473894.1:p.Thr7450Ile
  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.22349C>T
  hgvsp: ENSP00000416578.2:p.Thr7450Ile
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.217C>T
  hgvsp: ENSP00000389074.1:p.Thr73Ile
  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.22349C>T
  hgvsp: ENSP00000380505.3:p.Thr7450Ile
  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.6539C>T
  hgvsp: ENSP00000410961.1:p.Thr2180Ile
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr7450Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-152381058-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381058
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381058
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.213G>T
  hgvsp: ENSP00000389074.1:p.Ala72Ser
  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.22345G>T
  hgvsp: ENSP00000380505.3:p.Ala7449Ser
  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.17242G>T
  hgvsp: ENSP00000386259.1:p.Ala5748Ser
  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.6535G>T
  hgvsp: ENSP00000410961.1:p.Ala2179Ser
  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.22345G>T
  hgvsp: ENSP00000416578.2:p.Ala7449Ser
  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.17242G>T
  hgvsp: ENSP00000172853.10:p.Ala5748Ser
  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.22345G>T
  hgvsp: ENSP00000474498.1:p.Ala7449Ser
  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.22345G>T
  hgvsp: ENSP00000473894.1:p.Ala7449Ser
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala7449Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

2-152381062-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381062
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381062
    reference: chr 2
allele count: 11
allele frequency: 9.108674770627008e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000172853
  ensembl transcript: ENST00000172853
  gene symbol: NEB
  hgvsc: ENST00000172853.10:c.17238G>C
  hgvsp: ENSP00000172853.10:p.Lys5746Asn
  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.6531G>C
  hgvsp: ENSP00000410961.1:p.Lys2177Asn
  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.22341G>C
  hgvsp: ENSP00000416578.2:p.Lys7447Asn
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.209G>C
  hgvsp: ENSP00000389074.1:p.Lys70Asn
  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.22341G>C
  hgvsp: ENSP00000380505.3:p.Lys7447Asn
  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.17238G>C
  hgvsp: ENSP00000386259.1:p.Lys5746Asn
  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.22341G>C
  hgvsp: ENSP00000473894.1:p.Lys7447Asn
  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.22341G>C
  hgvsp: ENSP00000474498.1:p.Lys7447Asn
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2467
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13377
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys7447Asn
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

2-152381066-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381066
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381066
    reference: chr 2
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
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.22337T>C
  hgvsp: ENSP00000416578.2:p.Ile7446Thr
  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.22337T>C
  hgvsp: ENSP00000474498.1:p.Ile7446Thr
  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.6527T>C
  hgvsp: ENSP00000410961.1:p.Ile2176Thr
  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.17234T>C
  hgvsp: ENSP00000172853.10:p.Ile5745Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.205T>C
  hgvsp: ENSP00000389074.1:p.Ile69Thr
  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.22337T>C
  hgvsp: ENSP00000380505.3:p.Ile7446Thr
  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.22337T>C
  hgvsp: ENSP00000473894.1:p.Ile7446Thr
  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.17234T>C
  hgvsp: ENSP00000386259.1:p.Ile5745Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile7446Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

2-152381067-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381067
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381067
    reference: chr 2
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000386259
  ensembl transcript: ENST00000409198
  gene symbol: NEB
  hgvsc: ENST00000409198.1:c.17233A>G
  hgvsp: ENSP00000386259.1:p.Ile5745Val
  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.22336A>G
  hgvsp: ENSP00000473894.1:p.Ile7446Val
  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.22336A>G
  hgvsp: ENSP00000380505.3:p.Ile7446Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.204A>G
  hgvsp: ENSP00000389074.1:p.Ile69Val
  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.22336A>G
  hgvsp: ENSP00000416578.2:p.Ile7446Val
  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.17233A>G
  hgvsp: ENSP00000172853.10:p.Ile5745Val
  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.22336A>G
  hgvsp: ENSP00000474498.1:p.Ile7446Val
  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.6526A>G
  hgvsp: ENSP00000410961.1:p.Ile2176Val
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile7446Val
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-152381073-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381073
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381073
    reference: chr 2
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.198C>G
  hgvsp: ENSP00000389074.1:p.Pro67Ala
  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.17227C>G
  hgvsp: ENSP00000172853.10:p.Pro5743Ala
  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.22330C>G
  hgvsp: ENSP00000380505.3:p.Pro7444Ala
  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.22330C>G
  hgvsp: ENSP00000416578.2:p.Pro7444Ala
  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.22330C>G
  hgvsp: ENSP00000473894.1:p.Pro7444Ala
  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.17227C>G
  hgvsp: ENSP00000386259.1:p.Pro5743Ala
  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.22330C>G
  hgvsp: ENSP00000474498.1:p.Pro7444Ala
  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.6520C>G
  hgvsp: ENSP00000410961.1:p.Pro2174Ala
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36592
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro7444Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

2-152381073-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381073
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381073
    reference: chr 2
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
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.17227C>A
  hgvsp: ENSP00000386259.1:p.Pro5743Thr
  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.22330C>A
  hgvsp: ENSP00000380505.3:p.Pro7444Thr
  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.22330C>A
  hgvsp: ENSP00000416578.2:p.Pro7444Thr
  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.22330C>A
  hgvsp: ENSP00000473894.1:p.Pro7444Thr
  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.17227C>A
  hgvsp: ENSP00000172853.10:p.Pro5743Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.198C>A
  hgvsp: ENSP00000389074.1:p.Pro67Thr
  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.22330C>A
  hgvsp: ENSP00000474498.1:p.Pro7444Thr
  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.6520C>A
  hgvsp: ENSP00000410961.1:p.Pro2174Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro7444Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-152381092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381092
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381092
    reference: chr 2
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000473894
  ensembl transcript: ENST00000603639
  gene symbol: NEB
  hgvsc: ENST00000603639.1:c.22311C>T
  hgvsp: ENST00000603639.1:c.22311C>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.22311C>T
  hgvsp: ENST00000604864.1:c.22311C>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.17208C>T
  hgvsp: ENST00000409198.1:c.17208C>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.22311C>T
  hgvsp: ENST00000397345.3:c.22311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.179C>T
  hgvsp: ENST00000434685.1:c.179C>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.6501C>T
  hgvsp: ENST00000413693.1:c.6501C>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.22311C>T
  hgvsp: ENST00000427231.2:c.22311C>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.17208C>T
  hgvsp: ENST00000172853.10:c.17208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13893
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr7437Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

2-152381101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381101
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381101
    reference: chr 2
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.170C>T
  hgvsp: ENST00000434685.1:c.170C>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.22302C>T
  hgvsp: ENST00000603639.1:c.22302C>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.22302C>T
  hgvsp: ENST00000427231.2:c.22302C>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.17199C>T
  hgvsp: ENST00000172853.10:c.17199C>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.17199C>T
  hgvsp: ENST00000409198.1:c.17199C>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.22302C>T
  hgvsp: ENST00000604864.1:c.22302C>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.22302C>T
  hgvsp: ENST00000397345.3:c.22302C>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.6492C>T
  hgvsp: ENST00000413693.1:c.6492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn7434Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum

2-152381103-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381103
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381103
    reference: chr 2
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000410961
  ensembl transcript: ENST00000413693
  gene symbol: NEB
  hgvsc: ENST00000413693.1:c.6490A>T
  hgvsp: ENSP00000410961.1:p.Asn2164Tyr
  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.22300A>T
  hgvsp: ENSP00000380505.3:p.Asn7434Tyr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.168A>T
  hgvsp: ENSP00000389074.1:p.Asn57Tyr
  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.22300A>T
  hgvsp: ENSP00000416578.2:p.Asn7434Tyr
  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.22300A>T
  hgvsp: ENSP00000474498.1:p.Asn7434Tyr
  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.17197A>T
  hgvsp: ENSP00000386259.1:p.Asn5733Tyr
  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.22300A>T
  hgvsp: ENSP00000473894.1:p.Asn7434Tyr
  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.17197A>T
  hgvsp: ENSP00000172853.10:p.Asn5733Tyr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13376
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn7434Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-152381106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381106
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381106
    reference: chr 2
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22297G>A
  hgvsp: ENSP00000380505.3:p.Glu7433Lys
  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.6487G>A
  hgvsp: ENSP00000410961.1:p.Glu2163Lys
  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.17194G>A
  hgvsp: ENSP00000386259.1:p.Glu5732Lys
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.165G>A
  hgvsp: ENSP00000389074.1:p.Glu56Lys
  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.22297G>A
  hgvsp: ENSP00000474498.1:p.Glu7433Lys
  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.22297G>A
  hgvsp: ENSP00000473894.1:p.Glu7433Lys
  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.17194G>A
  hgvsp: ENSP00000172853.10:p.Glu5732Lys
  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.22297G>A
  hgvsp: ENSP00000416578.2:p.Glu7433Lys
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu7433Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

2-152381109-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381109
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381109
    reference: chr 2
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
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.22294A>G
  hgvsp: ENSP00000380505.3:p.Lys7432Glu
  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.22294A>G
  hgvsp: ENSP00000474498.1:p.Lys7432Glu
  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.22294A>G
  hgvsp: ENSP00000473894.1:p.Lys7432Glu
  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.17191A>G
  hgvsp: ENSP00000172853.10:p.Lys5731Glu
  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.17191A>G
  hgvsp: ENSP00000386259.1:p.Lys5731Glu
  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.6484A>G
  hgvsp: ENSP00000410961.1:p.Lys2162Glu
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.162A>G
  hgvsp: ENSP00000389074.1:p.Lys55Glu
  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.22294A>G
  hgvsp: ENSP00000416578.2:p.Lys7432Glu
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys7432Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

2-152381111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381111
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381111
    reference: chr 2
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
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.22292C>T
  hgvsp: ENSP00000380505.3:p.Ala7431Val
  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.22292C>T
  hgvsp: ENSP00000473894.1:p.Ala7431Val
  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.17189C>T
  hgvsp: ENSP00000172853.10:p.Ala5730Val
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.160C>T
  hgvsp: ENSP00000389074.1:p.Ala54Val
  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.17189C>T
  hgvsp: ENSP00000386259.1:p.Ala5730Val
  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.22292C>T
  hgvsp: ENSP00000416578.2:p.Ala7431Val
  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.22292C>T
  hgvsp: ENSP00000474498.1:p.Ala7431Val
  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.6482C>T
  hgvsp: ENSP00000410961.1:p.Ala2161Val
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2454
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala7431Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-152381122-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381122
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381122
    reference: chr 2
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000380505
  ensembl transcript: ENST00000397345
  gene symbol: NEB
  hgvsc: ENST00000397345.3:c.22281C>T
  hgvsp: ENST00000397345.3:c.22281C>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.17178C>T
  hgvsp: ENST00000409198.1:c.17178C>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.22281C>T
  hgvsp: ENST00000603639.1:c.22281C>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.22281C>T
  hgvsp: ENST00000427231.2:c.22281C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.149C>T
  hgvsp: ENST00000434685.1:c.149C>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.17178C>T
  hgvsp: ENST00000172853.10:c.17178C>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.6471C>T
  hgvsp: ENST00000413693.1:c.6471C>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.22281C>T
  hgvsp: ENST00000604864.1:c.22281C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13361
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr7427Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-152381127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 152381127
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 152381127
    reference: chr 2
allele count: 2
allele frequency: 1.656891009709381e-5
allele num: 120708
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.17173G>A
  hgvsp: ENSP00000386259.1:p.Ala5725Thr
  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.22276G>A
  hgvsp: ENSP00000474498.1:p.Ala7426Thr
  variant of: http://identifiers.org/hgnc/7720
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000183091
  ensembl protein: ENSP00000389074
  ensembl transcript: ENST00000434685
  gene symbol: NEB
  hgvsc: ENST00000434685.1:c.144G>A
  hgvsp: ENSP00000389074.1:p.Ala49Thr
  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.22276G>A
  hgvsp: ENSP00000380505.3:p.Ala7426Thr
  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.6466G>A
  hgvsp: ENSP00000410961.1:p.Ala2156Thr
  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.17173G>A
  hgvsp: ENSP00000172853.10:p.Ala5725Thr
  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.22276G>A
  hgvsp: ENSP00000473894.1:p.Ala7426Thr
  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.22276G>A
  hgvsp: ENSP00000416578.2:p.Ala7426Thr
  variant of: http://identifiers.org/hgnc/7720
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala7426Thr
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2272
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7145
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34052
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9133
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 7.198e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.231035e6

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9135
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7137
bin: 6.75e1
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: 3
allele frequency: 4.515624059244988e-5
allele num: 66436
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.0e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

DP
type: SiteQuality
SIO_000300: 2.229124e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 6.053e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2263
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9132
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-3

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.127e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.215764e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.057e0

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeQuality
all individuals: 507
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9131
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51758885482745e-5
allele num: 65894
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.461e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.293e0

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 2.20395e6

GenotypeQuality
all individuals: 760
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6670
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 934
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9133
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2102
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.083247687564234e-4
allele num: 9730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.044e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

DP
type: SiteQuality
SIO_000300: 2.174605e6

MQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

QD
type: SiteQuality
SIO_000300: 1.436e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 2939
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9135
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2868
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1232
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27827
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.080505898090721e-5
allele num: 16446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.055e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.174936e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

GenotypeQuality
all individuals: 765
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9135
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 373
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2939
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.048873441263453e-5
allele num: 65598
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.519267992257611e-4
allele num: 11366
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.055e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.174936e6

QD
type: SiteQuality
SIO_000300: 1.371e1

GenotypeQuality
all individuals: 840
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65590
num of homozygotes: 0

South Asian
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allele count: 12
allele frequency: 7.297494526879105e-4
allele num: 16444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.613e1

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.169102e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.235e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.029654036243822e-4
allele num: 9712
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.834e0

QD
type: SiteQuality
SIO_000300: 1.135e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 2.134676e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538319539734794e-5
allele num: 65006
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

DP
type: SiteQuality
SIO_000300: 2.101136e6

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

QD
type: SiteQuality
SIO_000300: 1.272e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64962
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.874e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.98e-1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.261e0

QD
type: SiteQuality
SIO_000300: 1.821e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.243e0

VQSLOD
type: SiteQuality
SIO_000300: -3.826e0

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

South Asian
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allele count: 1
allele frequency: 6.098304671301378e-5
allele num: 16398
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
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Latino
type: Population
allele count: 1
allele frequency: 8.934953538241601e-5
allele num: 11192
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.231223836493475e-4
allele num: 8122
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.181233774261343e-5
allele num: 16178
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Other
type: Population
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East Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
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MQRankSum
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ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 1.841283e6

QD
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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
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allele num: 16178
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65562
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African
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.107e1

ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1045
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65714
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
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allele num: 9726
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European (Finnish)
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allele count: 2
allele frequency: 3.036744609778318e-4
allele num: 6586
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Other
type: Population
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allele num: 884
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South Asian
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QD
type: SiteQuality
SIO_000300: 1.493e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.52012647452268e-5
allele num: 65784
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.335e0

FS
type: SiteQuality
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QD
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SIO_000300: 1.214e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.895011e6

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.026272577996716e-4
allele num: 9744
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515610791148833e-5
allele num: 65980
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.915346e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.083e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513821187441339e-5
allele num: 66058
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.179e0

VQSLOD
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BaseQRankSum
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SIO_000300: -4.269e0

MQ
type: SiteQuality
SIO_000300: 5.876e1

DP
type: SiteQuality
SIO_000300: 1.919853e6

QD
type: SiteQuality
SIO_000300: 1.19e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66386
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

QD
type: SiteQuality
SIO_000300: 1.694e1

DP
type: SiteQuality
SIO_000300: 1.941063e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.956e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.075e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

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: 896
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.259e0

MQ
type: SiteQuality
SIO_000300: 5.905e1

FS
type: SiteQuality
SIO_000300: 5.115e0

DP
type: SiteQuality
SIO_000300: 1.954728e6

VQSLOD
type: SiteQuality
SIO_000300: -2.916e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.885e0

QD
type: SiteQuality
SIO_000300: 4.85e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.73460537727667e-4
allele num: 11530
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.955938e6

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -2.88e-1

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.003301815998799e-5
allele num: 66630
num of homozygotes: 0

Other
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8598
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9800
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
type: SiteQuality
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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allele num: 8598
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South Asian
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BaseQRankSum
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
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DP
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ClippingRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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Other
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allele num: 898
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South Asian
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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QD
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36360
bin: 6.25e1
variant carriers: 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: 66720
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: 11570
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

QD
type: SiteQuality
SIO_000300: 1.091e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

FS
type: SiteQuality
SIO_000300: 2.978e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.827e0

DP
type: SiteQuality
SIO_000300: 1.961458e6

GenotypeQuality
all individuals: 563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
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: 8612
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.155e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

DP
type: SiteQuality
SIO_000300: 1.961624e6

MQRankSum
type: SiteQuality
SIO_000300: -1.162e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.391e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.437e0

GenotypeQuality
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bin: 9.25e1
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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bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 2780
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
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: 8612
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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.813e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.326e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 8.224e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

DP
type: SiteQuality
SIO_000300: 1.962086e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

QD
type: SiteQuality
SIO_000300: 1.0e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.019991840065279e-4
allele num: 9804
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 1.96231e6

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 1.037e1

GenotypeQuality
all individuals: 561
bin: 9.25e1
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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GenotypeQuality
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GenotypeQuality
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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: 3
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variant carriers: 0

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

African
type: Population
allele count: 5
allele frequency: 5.099959200326398e-4
allele num: 9804
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.296769166217107e-4
allele num: 66732
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

DP
type: SiteQuality
SIO_000300: 1.964781e6

QD
type: SiteQuality
SIO_000300: 1.25e1

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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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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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: 2779
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322340919647004e-4
allele num: 8612
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993766482857828e-5
allele num: 66736
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 1.817e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

DP
type: SiteQuality
SIO_000300: 1.964038e6

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

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

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 16512
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.76e0

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

VQSLOD
type: SiteQuality
SIO_000300: -2.175e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

DP
type: SiteQuality
SIO_000300: 1.96365e6

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: 1

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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: 9808
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

DP
type: SiteQuality
SIO_000300: 1.963772e6

FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

East Asian
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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MQ
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

African
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allele frequency: 0.0e0
allele num: 9808
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South Asian
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allele frequency: 1.816860465116279e-4
allele num: 16512
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Latino
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allele frequency: 0.0e0
allele num: 11574
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Latino
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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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South Asian
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allele num: 16512
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African
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16512
num of homozygotes: 1

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 5.993766482857828e-5
allele num: 66736
num of homozygotes: 0

Latino
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allele num: 11572
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East Asian
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European (Finnish)
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African
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Other
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South Asian
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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allele num: 66736
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East Asian
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African
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European (Finnish)
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Other
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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DP
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 9.75e1
variant carriers: 1

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: 66736
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.337e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 7.45e-1

DP
type: SiteQuality
SIO_000300: 1.964467e6

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.013e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
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: 9806
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: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.589e-1

DP
type: SiteQuality
SIO_000300: 1.964532e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 1.477e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

QD
type: SiteQuality
SIO_000300: 9.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 8608
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.964584e6

FS
type: SiteQuality
SIO_000300: 5.441e0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e-1

QD
type: SiteQuality
SIO_000300: 1.42e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
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: 2.4e0

DP
type: SiteQuality
SIO_000300: 1.964745e6

MQRankSum
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 5.536e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
SIO_000300: -1.535e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.572e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.04e-1

GenotypeQuality
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bin: 1.25e1
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
all individuals: 1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 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: 1.019575856443719e-4
allele num: 9808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 8610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 8.236000000000001e0

QD
type: SiteQuality
SIO_000300: 1.633e1

VQSLOD
type: SiteQuality
SIO_000300: -1.535e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

DP
type: SiteQuality
SIO_000300: 1.964796e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.180999999999999e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1097
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GenotypeQuality
all individuals: 2720
bin: 9.75e1
variant carriers: 4

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

South Asian
type: Population
allele count: 4
allele frequency: 2.42306760358614e-4
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: 8614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.654e0

MQ
type: SiteQuality
SIO_000300: 5.812e1

FS
type: SiteQuality
SIO_000300: 1.172e0

DP
type: SiteQuality
SIO_000300: 1.965688e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

QD
type: SiteQuality
SIO_000300: 1.406e1

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.815e0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1062
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 14
allele frequency: 1.440922190201729e-3
allele num: 9716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.631058968817536e-4
allele num: 6478
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: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 9.176796245035503e-4
allele num: 66472
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.30684e2

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

DP
type: SiteQuality
SIO_000300: 2.008396e6

MQ
type: SiteQuality
SIO_000300: 5.743e1

VQSLOD
type: SiteQuality
SIO_000300: -8.345999999999999e1

QD
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.579e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.29e0

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
all individuals: 539
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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allele num: 898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.796e1

FS
type: SiteQuality
SIO_000300: 2.945e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.087e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

DP
type: SiteQuality
SIO_000300: 1.98582e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.587e0

QD
type: SiteQuality
SIO_000300: 1.524e1

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
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.305e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.0e0

QD
type: SiteQuality
SIO_000300: 2.14e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

FS
type: SiteQuality
SIO_000300: 3.1151e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

DP
type: SiteQuality
SIO_000300: 1.985817e6

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
all individuals: 540
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 3159
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 2474
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GenotypeQuality
all individuals: 375
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e0

MQRankSum
type: SiteQuality
SIO_000300: 8.89e-1

DP
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SIO_000300: 1.986266e6

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.981e0

InbreedingCoeff
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SIO_000300: 2.1e-3

FS
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SIO_000300: 3.734e0

QD
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SIO_000300: 1.682e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.76e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.974e0

MQ
type: SiteQuality
SIO_000300: 5.631e1

ClippingRankSum
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SIO_000300: -2.264e0

BaseQRankSum
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VQSLOD
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QD
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DP
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ReadPosRankSum
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SIO_000300: 2.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.787e0

MQRankSum
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SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.456e1

MQ
type: SiteQuality
SIO_000300: 5.824e1

DP
type: SiteQuality
SIO_000300: 1.987084e6

InbreedingCoeff
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SIO_000300: 5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

FS
type: SiteQuality
SIO_000300: 6.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.778e0

QD
type: SiteQuality
SIO_000300: 1.257e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.732e0

MQRankSum
type: SiteQuality
SIO_000300: -1.667e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.807e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.653e0

VQSLOD
type: SiteQuality
SIO_000300: -2.527e0

DP
type: SiteQuality
SIO_000300: 1.987068e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 44

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: 898
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
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

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.443492073006263e-4
allele num: 66734
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

MQ
type: SiteQuality
SIO_000300: 5.755e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 6.09e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.345e-1

DP
type: SiteQuality
SIO_000300: 1.993482e6

MQRankSum
type: SiteQuality
SIO_000300: 7.65e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.23e-1

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
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: 9802
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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: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.23e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 4.49e0

DP
type: SiteQuality
SIO_000300: 1.988673e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.397e0

MQ
type: SiteQuality
SIO_000300: 5.761e1

QD
type: SiteQuality
SIO_000300: 1.237e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 1.775e0

MQ
type: SiteQuality
SIO_000300: 5.751e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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DP
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BaseQRankSum
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SIO_000300: -2.981e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
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SIO_000300: 1.26e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
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
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
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FS
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ReadPosRankSum
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QD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

MQ
type: SiteQuality
SIO_000300: 5.76e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 370
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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: 11
allele frequency: 6.661821705426356e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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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ReadPosRankSum
type: SiteQuality
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MQRankSum
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DP
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SIO_000300: 1.990209e6

MQ
type: SiteQuality
SIO_000300: 5.646e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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Latino
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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FS
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DP
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Other
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African
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European (Finnish)
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South Asian
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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Other
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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Other
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQ
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QD
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DP
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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South Asian
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QD
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.294e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

FS
type: SiteQuality
SIO_000300: 1.201e0

DP
type: SiteQuality
SIO_000300: 1.988614e6

QD
type: SiteQuality
SIO_000300: 1.108e1

MQ
type: SiteQuality
SIO_000300: 5.789e1

GenotypeQuality
all individuals: 36572
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
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: 11570
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.277e0

QD
type: SiteQuality
SIO_000300: 1.081e1

MQRankSum
type: SiteQuality
SIO_000300: -1.226e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

DP
type: SiteQuality
SIO_000300: 1.988396e6

VQSLOD
type: SiteQuality
SIO_000300: -2.568e0

FS
type: SiteQuality
SIO_000300: 1.541e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3146
bin: 7.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
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: 8624
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.905e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.012e1

FS
type: SiteQuality
SIO_000300: 2.076e0

MQRankSum
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
SIO_000300: 1.989256e6

VQSLOD
type: SiteQuality
SIO_000300: -2.317e0

MQ
type: SiteQuality
SIO_000300: 5.803e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1