1-148011027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011027
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011027
    reference: chr 1
allele count: 1
allele frequency: 1.987281399046105e-4
allele num: 5032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-863G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3055G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1476G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1612G>A
  hgvsp: ENSP00000309907.10:p.Gly538Glu
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2293G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+3054G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1595G>A
  hgvsp: ENSP00000358221.1:p.Gly532Glu
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2403G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29772
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5677
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly538Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

1-148011037-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011037
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011037
    reference: chr 1
allele count: 311
allele frequency: 6.292998785916633e-2
allele num: 4942
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1602G>C
  hgvsp: ENSP00000309907.10:p.Asp535His
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3065G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2283G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-873G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2413G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1585G>C
  hgvsp: ENSP00000358221.1:p.Asp529His
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+3044G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1466G>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 1.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30005
  bin: 2.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 7.5e0
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 2.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 1.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 60
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 5075
  bin: 2.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 28353
  bin: 7.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 6.75e1
  variant carriers: 26
hgvs: p.Asp535His
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum

1-148011047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011047
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011047
    reference: chr 1
allele count: 1
allele frequency: 1.906214258482653e-4
allele num: 5246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2423G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1575G>A
  hgvsp: ENST00000369219.1:c.1575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1456G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1592G>A
  hgvsp: ENST00000310701.10:c.1592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2273G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3075G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-883G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+3034G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25688
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg531Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

1-148011052-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011052
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011052
    reference: chr 1
allele count: 17
allele frequency: 3.21482602118003e-3
allele num: 5288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2268A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1451A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1570A>G
  hgvsp: ENSP00000358221.1:p.Ser524Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+3029A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1587A>G
  hgvsp: ENSP00000309907.10:p.Ser530Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-888A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2428A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3080A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 26836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25453
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser530Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

1-148011053-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011053
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011053
    reference: chr 1
allele count: 18
allele frequency: 3.392385978137957e-3
allele num: 5306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-889C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1569C>A
  hgvsp: ENST00000369219.1:c.1569C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1450C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3081C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2429C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1586C>A
  hgvsp: ENST00000310701.10:c.1586C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2267C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+3028C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu529Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-148011069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011069
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011069
    reference: chr 1
allele count: 246
allele frequency: 4.625799172621286e-2
allele num: 5318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1566-13C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3097C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2251C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1583-13C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1434C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-905C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+3012C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2445C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 1.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20747
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.5e0
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 9.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 6.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 46
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

1-148011082-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011082
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011082
    reference: chr 1
allele count: 2
allele frequency: 3.306878306878307e-4
allele num: 6048
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2458T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-918T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2238T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2999T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1583-26T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3110T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1566-26T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1421T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4107
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-148011090-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011090
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011090
    reference: chr 1
allele count: 1
allele frequency: 1.653986106516705e-4
allele num: 6046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2230C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1583-34C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2991C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3118C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1413C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-926C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1566-34C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2466C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4437
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

1-148011098-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011098
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011098
    reference: chr 1
allele count: 1
allele frequency: 1.606683804627249e-4
allele num: 6224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2222G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2474G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2983G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3126G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-934G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1583-42G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1566-42G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1405G>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16692
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4773
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-148011102-A-AACCAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011102
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011107
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 6336
alternate allele: AACCAC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-943_1039-939dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1583-51_1583-47dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2483_1039-2479dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1566-51_1566-47dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2213_1315+2217dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2974_1263+2978dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3135_1091-3131dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1396_1488+1400dupGTGGT
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16933
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4946
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

1-148011106-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011106
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011106
    reference: chr 1
allele count: 2243
allele frequency: 4.351959642995731e-1
allele num: 5154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2975T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+1397T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1583-50T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-2482T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+2214T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1566-50T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-942T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1091-3134T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.25e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 7.5e0
  variant carriers: 596
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 1.25e1
  variant carriers: 890
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.75e1
  variant carriers: 548
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 2.5e0
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.25e1
  variant carriers: 149
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.75e1
  variant carriers: 177
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 1.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 73
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 1.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.25e1
  variant carriers: 151
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 36
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

1-148011629-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011629
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011629
    reference: chr 1
allele count: 1
allele frequency: 9.860571518725226e-6
allele num: 101414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1465A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1691A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+874A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+51A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2452A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3225A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3005A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+51A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6761
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

1-148011630-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011630
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011630
    reference: chr 1
allele count: 1
allele frequency: 9.861543923316634e-6
allele num: 101404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1690A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+50A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3224A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+50A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2451A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3006A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1466A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+873A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9714
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6760
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-148011632-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011632
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011632
    reference: chr 1
allele count: 4
allele frequency: 3.944773175542406e-5
allele num: 101400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1688G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3008G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+48G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2449G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3222G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1468G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+871G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+48G>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2953
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

1-148011635-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011635
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011635
    reference: chr 1
allele count: 1
allele frequency: 9.862321985088169e-6
allele num: 101396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+45G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+45G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3219G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2446G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1471G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1685G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3011G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+868G>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7853
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6753
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

1-148011636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011636
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011636
    reference: chr 1
allele count: 2
allele frequency: 1.972503303943034e-5
allele num: 101394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+44G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1684G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1472G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3218G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2445G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+44G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+867G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3012G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3058
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

1-148011637-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011637
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011637
    reference: chr 1
allele count: 1
allele frequency: 9.862321985088169e-6
allele num: 101396
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+43T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1683T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3217T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3013T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1473T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2444T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+43T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+866T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

1-148011638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011638
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011638
    reference: chr 1
allele count: 1
allele frequency: 9.861932938856015e-6
allele num: 101400
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+42C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3216C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+42C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1682C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2443C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3014C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+865C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1474C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-148011640-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011640
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011640
    reference: chr 1
allele count: 3
allele frequency: 2.958404828116679e-5
allele num: 101406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1680A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+863A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2441A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+40A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3016A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1476A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+40A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3214A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7853
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-148011641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011641
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011641
    reference: chr 1
allele count: 19
allele frequency: 1.873915101783178e-4
allele num: 101392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3017C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1477C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2440C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+862C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+39C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+39C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3213C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1679C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22384
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-148011641-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011641
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011641
    reference: chr 1
allele count: 2
allele frequency: 1.972542212403345e-5
allele num: 101392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1679C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+39C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+39C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3213C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1477C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3017C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2440C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+862C>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3765
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6737
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9739
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

1-148011653-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011653
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011653
    reference: chr 1
allele count: 1
allele frequency: 9.86212745813527e-6
allele num: 101398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2428A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1489A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+850A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+27A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3029A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3201A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1667A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+27A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3612
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22479
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

1-148011657-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011657
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011657
    reference: chr 1
allele count: 1
allele frequency: 9.859988168014199e-6
allele num: 101420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+846C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1493C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1663C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3033C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+23C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2424C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+23C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3197C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3388
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-148011658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011658
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011658
    reference: chr 1
allele count: 1
allele frequency: 9.859599305884209e-6
allele num: 101424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2423G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3196G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3034G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+845G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1494G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+22G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+22G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1662G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3608
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

1-148011660-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011660
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011660
    reference: chr 1
allele count: 1
allele frequency: 9.859599305884209e-6
allele num: 101424
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1660A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3194A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+20A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1496A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+20A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2421A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3036A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+843A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/1-148011661-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011661
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011661
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 101404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1497G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1659G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+842G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+19G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+19G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2420G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3037G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3193G>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3389
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3609
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22540
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-148011661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011661
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011661
    reference: chr 1
allele count: 1
allele frequency: 9.861543923316634e-6
allele num: 101404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2420G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+842G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+19G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1659G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1497G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+19G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3037G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3193G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3609
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2928
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9759
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-148011662-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011662
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011662
    reference: chr 1
allele count: 3
allele frequency: 2.959163543105149e-5
allele num: 101380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3192G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2419G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3038G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+18G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1498G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1658G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+841G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+18G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9762
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

1-148011666-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011666
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011666
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 101404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1502T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+837T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+14T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3042T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3188T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+14T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2415T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1654T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6712
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-148011668-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011668
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011667
    reference: chr 1
allele count: 2
allele frequency: 1.972425491627054e-5
allele num: 101398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1651delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+834delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2412delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3185delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+11delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1505delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3045delC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+11delC
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3609
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: TG
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

1-148011668-TGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011668
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011666
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 101398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+10_1582+11delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+833_1488+834delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1650_1315+1651delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3046_1039-3045delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3184_1090+3185delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2411_1263+2412delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+10_1565+11delGC
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1506_1039-1505delGC
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3090
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3609
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: TGC
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-148011669-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011669
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011669
    reference: chr 1
allele count: 2
allele frequency: 1.973593321360201e-5
allele num: 101338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+11C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3045C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1505C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3185C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+11C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1651C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2412C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+834C>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22512
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

1-148011669-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011669
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011669
    reference: chr 1
allele count: 1
allele frequency: 9.867966606801003e-6
allele num: 101338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1505C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+11C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1651C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+834C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3045C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2412C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3185C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+11C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9762
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22512
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-148011670-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011670
    reference: chr 1
allele count: 15
allele frequency: 1.485678063468167e-4
allele num: 100964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2411G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3046G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1650G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1506G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+10G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3184G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+10G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+833G>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2471
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9760
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

1-148011670-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011671
    reference: chr 1
allele count: 42
allele frequency: 4.159898577710867e-4
allele num: 100964
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2410_1263+2411insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+9_1582+10insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3047_1039-3046insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3183_1090+3184insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+832_1488+833insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1507_1039-1506insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+9_1565+10insA
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1649_1315+1650insA
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 2.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2471
  bin: 7.5e0
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 4
num of homozygotes: 10
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

1-148011670-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011670
    reference: chr 1
allele count: 348
allele frequency: 3.446773107246147e-3
allele num: 100964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1650G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3184G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3046G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+10G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2411G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1506G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+10G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+833G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 9.75e1
  variant carriers: 333
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9760
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

1-148011671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011671
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011671
    reference: chr 1
allele count: 1218
allele frequency: 1.207494795281055e-2
allele num: 100870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1507C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+9C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3183C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3047C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1649C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+9C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2410C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+832C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 9.75e1
  variant carriers: 1204
genotype quality: GenotypeQuality
  all individuals: 9810
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22682
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 9.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3632
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 2.5e0
  variant carriers: 5
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

1-148011671-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011671
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011671
    reference: chr 1
allele count: 20
allele frequency: 1.982750074353128e-4
allele num: 100870
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+9C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1649C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2410C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1507C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3047C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+9C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+832C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3183C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 2.5e0
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 7.5e0
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9810
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22682
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

1-148011672-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011672
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011672
    reference: chr 1
allele count: 16
allele frequency: 1.58084021657511e-4
allele num: 101212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2409T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+831T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+8T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3182T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1648T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3048T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+8T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1508T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 2.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9366
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10100
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 23337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.5e0
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.25e1
  variant carriers: 1
hgvs: c.1582+8T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-148011672-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011672
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011669
    reference: chr 1
allele count: 14
allele frequency: 1.383235189503221e-4
allele num: 101212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3179_1090+3181delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+828_1488+830delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+5_1582+7delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3051_1039-3049delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+5_1565+7delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2406_1263+2408delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1511_1039-1509delCTT
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1645_1315+1647delCTT
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6734
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1582+5_1582+7delCTT
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: AAAG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD

1-148011677-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011677
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011677
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 101096
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1582+3G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3053G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1643G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3177G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1565+3G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2404G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+826G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1513G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10109
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1582+3G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

1-148011682-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011682
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011682
    reference: chr 1
allele count: 2
allele frequency: 1.981296560469171e-5
allele num: 100944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1638C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3058C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2399C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1563C>T
  hgvsp: ENST00000369219.1:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+821C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3172C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1580C>T
  hgvsp: ENST00000310701.10:c.1580C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1518C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5083
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1580C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

1-148011683-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011683
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011683
    reference: chr 1
allele count: 1
allele frequency: 9.906875371507827e-6
allele num: 100940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2398C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1637C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1579C>G
  hgvsp: ENSP00000309907.10:p.Pro527Arg
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3171C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1519C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1562C>G
  hgvsp: ENSP00000358221.1:p.Pro521Arg
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3059C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+820C>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro527Arg
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

1-148011684-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011684
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011684
    reference: chr 1
allele count: 10
allele frequency: 9.907660603178377e-5
allele num: 100932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3060C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1636C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1578C>T
  hgvsp: ENSP00000309907.10:p.Pro527Ser
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+819C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3170C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1561C>T
  hgvsp: ENSP00000358221.1:p.Pro521Ser
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2397C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1520C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5079
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 10068
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro527Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

1-148011687-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011687
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011687
    reference: chr 1
allele count: 1
allele frequency: 9.912571122697806e-6
allele num: 100882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3167T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1558T>C
  hgvsp: ENSP00000358221.1:p.Cys520Arg
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+816T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1575T>C
  hgvsp: ENSP00000309907.10:p.Cys526Arg
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3063T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1633T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2394T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1523T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys526Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-148011689-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011689
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011689
    reference: chr 1
allele count: 3
allele frequency: 2.976426700531788e-5
allele num: 100792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1525C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3165C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+814C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1573C>A
  hgvsp: ENSP00000309907.10:p.Pro525Gln
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2392C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1556C>A
  hgvsp: ENSP00000358221.1:p.Pro519Gln
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1631C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3065C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3286
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2975
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro525Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

1-148011693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011693
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011693
    reference: chr 1
allele count: 1
allele frequency: 9.929697740000794e-6
allele num: 100708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1627C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2388C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1552C>T
  hgvsp: ENSP00000358221.1:p.Pro518Ser
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3069C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1529C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1569C>T
  hgvsp: ENSP00000309907.10:p.Pro524Ser
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+810C>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3161C>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22977
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2972
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro524Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

1-148011693-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011693
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011693
    reference: chr 1
allele count: 2
allele frequency: 1.985939548000159e-5
allele num: 100708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3161C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2388C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1627C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+810C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3069C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1529C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1552C>A
  hgvsp: ENSP00000358221.1:p.Pro518Thr
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1569C>A
  hgvsp: ENSP00000309907.10:p.Pro524Thr
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5066
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2972
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro524Thr
num of homozygotes: 1
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

1-148011695-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011695
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011695
    reference: chr 1
allele count: 1
allele frequency: 9.934827531394055e-6
allele num: 100656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1531A>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1567A>C
  hgvsp: ENSP00000309907.10:p.Asn523Thr
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1625A>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2386A>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+808A>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3159A>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1550A>C
  hgvsp: ENSP00000358221.1:p.Asn517Thr
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3071A>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5063
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn523Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-148011695-TTTTGATCTTCTTCCCCTTCTTTTCTTCCCCTTCTTCTTTCCTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011695
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011651
    reference: chr 1
allele count: 10
allele frequency: 9.934827531394055e-5
allele num: 100656
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsp: ENSP00000309907.10:p.Lys509ProfsTer13
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsp: ENSP00000358221.1:p.Lys503ProfsTer13
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys509ProfsTer13
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: TTTTGATCTTCTTCCCCTTCTTTTCTTCCCCTTCTTCTTTCCTTC
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

1-148011699-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011699
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011699
    reference: chr 1
allele count: 1
allele frequency: 9.946092180382328e-6
allele num: 100542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+804C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1563C>A
  hgvsp: ENSP00000309907.10:p.Gln522Lys
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2382C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1621C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3075C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1535C>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1546C>A
  hgvsp: ENSP00000358221.1:p.Gln516Lys
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3155C>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln522Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-148011699-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011699
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011699
    reference: chr 1
allele count: 1
allele frequency: 9.946092180382328e-6
allele num: 100542
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1563C>G
  hgvsp: ENSP00000309907.10:p.Gln522Glu
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1621C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1535C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1546C>G
  hgvsp: ENSP00000358221.1:p.Gln516Glu
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2382C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3075C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3155C>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+804C>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9931
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln522Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

1-148011700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011700
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011700
    reference: chr 1
allele count: 3
allele frequency: 2.984361943416497e-5
allele num: 100524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1536T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1620T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3076T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1562T>C
  hgvsp: ENST00000310701.10:c.1562T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3154T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+803T>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1545T>C
  hgvsp: ENST00000369219.1:c.1545T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2381T>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22533
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp521Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

1-148011701-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011701
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011701
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 100494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+802A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1561A>G
  hgvsp: ENSP00000309907.10:p.Asp521Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3077A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1544A>G
  hgvsp: ENSP00000358221.1:p.Asp515Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1619A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1537A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3153A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2380A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3015
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22436
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp521Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

1-148011702-CTTCTTCCCCTTCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011702
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011688
    reference: chr 1
allele count: 3
allele frequency: 2.994251038007026e-5
allele num: 100192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsp: ENSP00000358221.1:p.Lys510ArgfsTer16
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsp: ENSP00000309907.10:p.Lys516ArgfsTer16
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22002
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2747
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys516ArgfsTer16
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CTTCTTCCCCTTCTT
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

1-148011703-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011703
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011703
    reference: chr 1
allele count: 2
allele frequency: 1.995808801516815e-5
allele num: 100210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1542A>T
  hgvsp: ENSP00000358221.1:p.Glu514Asp
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1617A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1559A>T
  hgvsp: ENSP00000309907.10:p.Glu520Asp
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2378A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+800A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3151A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1539A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3079A>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu520Asp
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

1-148011704-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011704
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011704
    reference: chr 1
allele count: 5
allele frequency: 4.98932284910292e-5
allele num: 100214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3080A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+799A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2377A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1616A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1540A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1541A>G
  hgvsp: ENSP00000358221.1:p.Glu514Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1558A>G
  hgvsp: ENSP00000309907.10:p.Glu520Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3150A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9633
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5043
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Glu520Gly
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

1-148011706-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011706
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011706
    reference: chr 1
allele count: 1
allele frequency: 9.989211651416471e-6
allele num: 100108
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1556A>G
  hgvsp: ENST00000310701.10:c.1556A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3148A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3082A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1539A>G
  hgvsp: ENST00000369219.1:c.1539A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+797A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1614A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2375A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1542A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2858
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu519Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/1-148011708-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011708
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011708
    reference: chr 1
allele count: 1
allele frequency: 9.98861298120143e-6
allele num: 100114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2373G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3146G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1554G>T
  hgvsp: ENSP00000309907.10:p.Glu519Ter
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1537G>T
  hgvsp: ENSP00000358221.1:p.Glu513Ter
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3084G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+795G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1544G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1612G>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3559
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu519Ter
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-148011709-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011709
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011709
    reference: chr 1
allele count: 1
allele frequency: 1.000540291757549e-5
allele num: 99946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1536G>T
  hgvsp: ENST00000369219.1:c.1536G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+794G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1553G>T
  hgvsp: ENST00000310701.10:c.1553G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2372G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1545G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3145G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3085G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1611G>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2517
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9532
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly518Gly
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: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: FS

1-148011710-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011707
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 99928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1549_1039-1547delAAG
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3141_1090+3143delAAG
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1532_1534delAAG
  hgvsp: ENSP00000358221.1:p.Glu511del
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+790_1488+792delAAG
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1549_1551delAAG
  hgvsp: ENSP00000309907.10:p.Glu517del
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2368_1263+2370delAAG
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3089_1039-3087delAAG
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1607_1315+1609delAAG
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu517del
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: CCTT
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-148011710-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
allele count: 1
allele frequency: 1.000720518773517e-5
allele num: 99928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1610G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1546G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3144G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3086G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2371G>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1552G>T
  hgvsp: ENSP00000309907.10:p.Gly518Val
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1535G>T
  hgvsp: ENSP00000358221.1:p.Gly512Val
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+793G>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 1
hgvs: p.Gly518Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

1-148011710-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
allele count: 1
allele frequency: 1.000720518773517e-5
allele num: 99928
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1552G>C
  hgvsp: ENSP00000309907.10:p.Gly518Ala
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2371G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3144G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+793G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1610G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1535G>C
  hgvsp: ENSP00000358221.1:p.Gly512Ala
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1546G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3086G>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly518Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-148011710-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011710
    reference: chr 1
allele count: 1
allele frequency: 1.000720518773517e-5
allele num: 99928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2371G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1610G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1552G>A
  hgvsp: ENSP00000309907.10:p.Gly518Glu
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1546G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3086G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1535G>A
  hgvsp: ENSP00000358221.1:p.Gly512Glu
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3144G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+793G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3550
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly518Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

1-148011716-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011716
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011716
    reference: chr 1
allele count: 3
allele frequency: 3.031650430494361e-5
allele num: 98956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3138A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2365A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1552A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1546A>T
  hgvsp: ENSP00000309907.10:p.Lys516Ile
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+787A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1529A>T
  hgvsp: ENSP00000358221.1:p.Lys510Ile
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1604A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3092A>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5022
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys516Ile
num of homozygotes: 1
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

1-148011719-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011719
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011719
    reference: chr 1
allele count: 1
allele frequency: 1.025641025641026e-5
allele num: 97500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3135G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1526G>A
  hgvsp: ENSP00000358221.1:p.Arg509Lys
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3095G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1555G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1543G>A
  hgvsp: ENSP00000309907.10:p.Arg515Lys
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+784G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2362G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1601G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2682
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg515Lys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

1-148011721-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011721
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011721
    reference: chr 1
allele count: 1
allele frequency: 1.025956704627065e-5
allele num: 97470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1599A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1557A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1541A>T
  hgvsp: ENST00000310701.10:c.1541A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1524A>T
  hgvsp: ENST00000369219.1:c.1524A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3133A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2360A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3097A>T
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+782A>T
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2212
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2736
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly514Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

1-148011725-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011725
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011725
    reference: chr 1
allele count: 2
allele frequency: 2.116939751894661e-5
allele num: 94476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+778G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3101G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2356G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1561G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3129G>A
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1537G>A
  hgvsp: ENSP00000309907.10:p.Arg513Lys
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1520G>A
  hgvsp: ENSP00000358221.1:p.Arg507Lys
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1595G>A
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3127
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5001
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg513Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

1-148011731-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011731
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011731
    reference: chr 1
allele count: 2
allele frequency: 2.437775773384364e-5
allele num: 82042
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1531G>C
  hgvsp: ENSP00000309907.10:p.Arg511Thr
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1514G>C
  hgvsp: ENSP00000358221.1:p.Arg505Thr
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2350G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+772G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1589G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3107G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1567G>C
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3123G>C
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4863
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14862
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg511Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

1-148011734-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011734
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011734
    reference: chr 1
allele count: 1
allele frequency: 1.258019876714052e-5
allele num: 79490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsc: ENST00000369219.1:c.1511A>G
  hgvsp: ENSP00000358221.1:p.Glu504Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  hgvsc: ENST00000431121.1:c.1039-3110A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsc: ENST00000310701.10:c.1528A>G
  hgvsp: ENSP00000309907.10:p.Glu510Gly
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  hgvsc: ENST00000392972.3:c.1488+769A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  hgvsc: ENST00000444640.1:c.1039-1570A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  hgvsc: ENST00000458135.1:c.1315+1586A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  hgvsc: ENST00000436356.1:c.1090+3120A>G
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  hgvsc: ENST00000448574.1:c.1263+2347A>G
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5338
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu510Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-148011734-TCCTTCTTTGATCTTCTTCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 148011734
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 148011715
    reference: chr 1
allele count: 1
allele frequency: 1.258019876714052e-5
allele num: 79490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000376698
  ensembl transcript: ENST00000392972
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000358221
  ensembl transcript: ENST00000369219
  gene symbol: NBPF14
  hgvsp: ENSP00000358221.1:p.Gly498LysfsTer50
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000403155
  ensembl transcript: ENST00000431121
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000309907
  ensembl transcript: ENST00000310701
  gene symbol: NBPF14
  hgvsp: ENSP00000309907.10:p.Gly504LysfsTer50
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000416860
  ensembl transcript: ENST00000448574
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000411975
  ensembl transcript: ENST00000436356
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000410336
  ensembl transcript: ENST00000458135
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000396201
  ensembl transcript: ENST00000426874
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122497
  ensembl protein: ENSP00000397707
  ensembl transcript: ENST00000444640
  gene symbol: NBPF14
  variant of: http://identifiers.org/hgnc/25232
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly504LysfsTer50
num of homozygotes: 0
reference allele: TCCTTCTTTGATCTTCTTCC

GenotypeQuality
all individuals: 374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.516711833785004e-4
allele num: 2214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 958
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.588e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 9.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

VQSLOD
type: SiteQuality
SIO_000300: -5.183e0

FS
type: SiteQuality
SIO_000300: 2.1269e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

MQ
type: SiteQuality
SIO_000300: 2.9e1

DP
type: SiteQuality
SIO_000300: 1.79996e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.400000000000001e-2

GenotypeQuality
all individuals: 685
bin: 1.75e1
variant carriers: 18

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 21

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2601
bin: 2.5e0
variant carriers: 5

GenotypeQuality
all individuals: 70
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 550
bin: 6.25e1
variant carriers: 29

GenotypeQuality
all individuals: 256
bin: 9.75e1
variant carriers: 95

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 36

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 20

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 25

GenotypeQuality
all individuals: 47
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 266
bin: 3.25e1
variant carriers: 16

South Asian
type: Population
allele count: 34
allele frequency: 2.796052631578947e-2
allele num: 1216
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.19047619047619e-1
allele num: 168
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 1.188811188811189e-1
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 200
allele frequency: 1.007049345417926e-1
allele num: 1986
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.908396946564885e-3
allele num: 1048
num of homozygotes: 0

East Asian
type: Population
allele count: 17
allele frequency: 1.118421052631579e-1
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.651162790697674e-2
allele num: 86
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.959999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.886e2

FS
type: SiteQuality
SIO_000300: 2.92531e2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 2.607e1

DP
type: SiteQuality
SIO_000300: 1.76903e5

QD
type: SiteQuality
SIO_000300: 3.78e0

MQRankSum
type: SiteQuality
SIO_000300: -2.383e0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4716
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.5662100456621e-4
allele num: 2190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

VQSLOD
type: SiteQuality
SIO_000300: -3.238e0

QD
type: SiteQuality
SIO_000300: 7.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.47e-2

MQ
type: SiteQuality
SIO_000300: 2.898e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

DP
type: SiteQuality
SIO_000300: 1.63063e5

GenotypeQuality
all individuals: 1865
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4876
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 104
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 9.615384615384616e-4
allele num: 1040
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.15307582260372e-4
allele num: 1398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.204819277108434e-2
allele num: 166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.123595505617977e-2
allele num: 178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 5.111524163568773e-3
allele num: 2152
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

FS
type: SiteQuality
SIO_000300: 1.51123e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.649999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.065e2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.003e0

MQ
type: SiteQuality
SIO_000300: 2.645e1

DP
type: SiteQuality
SIO_000300: 1.62269e5

QD
type: SiteQuality
SIO_000300: 3.8e0

GenotypeQuality
all individuals: 45
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4807
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 223
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 43
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25004
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.092198581560284e-4
allele num: 1410
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.204819277108434e-2
allele num: 166
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.111111111111111e-2
allele num: 180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 9.596928982725527e-4
allele num: 1042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 5.58659217877095e-3
allele num: 2148
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.77e0

MQ
type: SiteQuality
SIO_000300: 2.645e1

VQSLOD
type: SiteQuality
SIO_000300: -1.126e2

FS
type: SiteQuality
SIO_000300: 1.55415e2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.547e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.66e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.985e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 1.60996e5

GenotypeQuality
all individuals: 3903
bin: 2.5e0
variant carriers: 9

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 22

GenotypeQuality
all individuals: 4045
bin: 2.25e1
variant carriers: 16

GenotypeQuality
all individuals: 51
bin: 7.25e1
variant carriers: 22

GenotypeQuality
all individuals: 55
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 341
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 24

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 369
bin: 3.25e1
variant carriers: 12

GenotypeQuality
all individuals: 17770
bin: 7.5e0
variant carriers: 11

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 10

GenotypeQuality
all individuals: 100
bin: 6.75e1
variant carriers: 22

European (Non-Finnish)
type: Population
allele count: 173
allele frequency: 9.001040582726327e-2
allele num: 1922
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 9.736540664375716e-3
allele num: 1746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.941747572815534e-3
allele num: 1030
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 9.243697478991597e-2
allele num: 238
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.388888888888889e-2
allele num: 72
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.176470588235294e-1
allele num: 136
num of homozygotes: 0

East Asian
type: Population
allele count: 15
allele frequency: 8.620689655172414e-2
allele num: 174
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.706e0

FS
type: SiteQuality
SIO_000300: 2.64403e2

MQ
type: SiteQuality
SIO_000300: 2.816e1

VQSLOD
type: SiteQuality
SIO_000300: -3.165e2

QD
type: SiteQuality
SIO_000300: 2.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

DP
type: SiteQuality
SIO_000300: 1.48024e5

GenotypeQuality
all individuals: 503
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3920
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 14040
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 458
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 8.0e-3
allele num: 250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1018
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 2.516e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.24e-2

DP
type: SiteQuality
SIO_000300: 1.35677e5

VQSLOD
type: SiteQuality
SIO_000300: -4.93e0

QD
type: SiteQuality
SIO_000300: 4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.3539e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeQuality
all individuals: 39
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4046
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 1

GenotypeQuality
all individuals: 566
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 2.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2138
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.524886877828054e-4
allele num: 2210
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.7268e1

VQSLOD
type: SiteQuality
SIO_000300: -5.255e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

MQRankSum
type: SiteQuality
SIO_000300: -1.893e0

QD
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 2.758e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.110000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.34371e5

GenotypeQuality
all individuals: 707
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12061
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 99
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 7.75e1
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GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.397537379067722e-4
allele num: 2274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 3.4466e1

DP
type: SiteQuality
SIO_000300: 1.33579e5

MQ
type: SiteQuality
SIO_000300: 3.202e1

VQSLOD
type: SiteQuality
SIO_000300: -9.635e0

MQRankSum
type: SiteQuality
SIO_000300: -2.718e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

GenotypeQuality
all individuals: 12093
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.55e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.649e-1

QD
type: SiteQuality
SIO_000300: 3.489e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 3.774e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

DP
type: SiteQuality
SIO_000300: 1.35464e5

GenotypeQuality
all individuals: 216
bin: 7.25e1
variant carriers: 215

GenotypeQuality
all individuals: 183
bin: 6.25e1
variant carriers: 171

GenotypeQuality
all individuals: 6118
bin: 7.5e0
variant carriers: 58

GenotypeQuality
all individuals: 13007
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 80

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 32

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 102

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 107

GenotypeQuality
all individuals: 201
bin: 6.75e1
variant carriers: 198

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 153

GenotypeQuality
all individuals: 602
bin: 2.25e1
variant carriers: 51

GenotypeQuality
all individuals: 1122
bin: 9.75e1
variant carriers: 1122

Other
type: Population
allele count: 36
allele frequency: 4.5e-1
allele num: 80
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 792
allele frequency: 4.313725490196079e-1
allele num: 1836
num of homozygotes: 0

African
type: Population
allele count: 107
allele frequency: 4.692982456140351e-1
allele num: 228
num of homozygotes: 0

East Asian
type: Population
allele count: 75
allele frequency: 4.518072289156627e-1
allele num: 166
num of homozygotes: 0

South Asian
type: Population
allele count: 785
allele frequency: 4.179978700745474e-1
allele num: 1878
num of homozygotes: 0

Latino
type: Population
allele count: 56
allele frequency: 4.827586206896552e-1
allele num: 116
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 392
allele frequency: 4.611764705882353e-1
allele num: 850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.51479e5

FS
type: SiteQuality
SIO_000300: 1.162e0

VQSLOD
type: SiteQuality
SIO_000300: 6.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

MQ
type: SiteQuality
SIO_000300: 3.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.929e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 4.9e0

GenotypeQuality
all individuals: 9712
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21998
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.986019572598362e-5
allele num: 10014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 6.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.03e0

MQ
type: SiteQuality
SIO_000300: 4.064e1

DP
type: SiteQuality
SIO_000300: 2.555714e6

QD
type: SiteQuality
SIO_000300: 6.7e-1

GenotypeQuality
all individuals: 125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 22029
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 151
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variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.744774400669994e-5
allele num: 57314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14820
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -2.692e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 4.971e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.013e0

MQ
type: SiteQuality
SIO_000300: 4.095e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 2.555329e6

GenotypeQuality
all individuals: 22131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6757
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 342
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.077430820005078e-4
allele num: 7878
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 4.103e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 2.55528e6

VQSLOD
type: SiteQuality
SIO_000300: -2.614e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

FS
type: SiteQuality
SIO_000300: 7.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeQuality
all individuals: 3059
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
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variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 22248
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GenotypeQuality
all individuals: 382
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variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.745139785696834e-5
allele num: 57302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.151e1

FS
type: SiteQuality
SIO_000300: 4.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.377e0

DP
type: SiteQuality
SIO_000300: 2.553985e6

QD
type: SiteQuality
SIO_000300: 3.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.004e0

GenotypeQuality
all individuals: 2914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
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GenotypeQuality
all individuals: 6750
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9724
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22261
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.988014382740711e-5
allele num: 10012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.745139785696834e-5
allele num: 57302
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

QD
type: SiteQuality
SIO_000300: 3.51e0

DP
type: SiteQuality
SIO_000300: 2.553745e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.825e0

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.233e0

MQ
type: SiteQuality
SIO_000300: 4.269e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

FS
type: SiteQuality
SIO_000300: 6.16e-1

GenotypeQuality
all individuals: 6749
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22309
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variant carriers: 0

GenotypeQuality
all individuals: 536
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GenotypeQuality
all individuals: 337
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 1040
bin: 2.25e1
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GenotypeQuality
all individuals: 9726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
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variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.745017973685129e-5
allele num: 57306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e-2

DP
type: SiteQuality
SIO_000300: 2.553825e6

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.667e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQ
type: SiteQuality
SIO_000300: 4.077e1

GenotypeQuality
all individuals: 3155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 8.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6748
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 9729
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22331
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.745017973685129e-5
allele num: 57306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

MQ
type: SiteQuality
SIO_000300: 4.29e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.566e0

DP
type: SiteQuality
SIO_000300: 2.553753e6

MQRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.5e0
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GenotypeQuality
all individuals: 121
bin: 2.75e1
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GenotypeQuality
all individuals: 6747
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GenotypeQuality
all individuals: 147
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GenotypeQuality
all individuals: 22359
bin: 6.25e1
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GenotypeQuality
all individuals: 967
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GenotypeQuality
all individuals: 1403
bin: 9.25e1
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GenotypeQuality
all individuals: 2919
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GenotypeQuality
all individuals: 9735
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GenotypeQuality
all individuals: 3611
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.234871222167935e-5
allele num: 57308
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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SIO_000300: -2.96e-1

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

MQ
type: SiteQuality
SIO_000300: 4.047e1

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7878
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10012
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European (Non-Finnish)
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allele count: 19
allele frequency: 3.315997067960487e-4
allele num: 57298
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 2.538715410002539e-4
allele num: 7878
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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DP
type: SiteQuality
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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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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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.743088334457182e-5
allele num: 14830
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57300
num of homozygotes: 0

FS
type: SiteQuality
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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SIO_000300: 3.85e0

InbreedingCoeff
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SIO_000300: -4.3e-3

MQ
type: SiteQuality
SIO_000300: 4.188e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

South Asian
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allele frequency: 6.742179072276159e-5
allele num: 14832
num of homozygotes: 0

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

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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DP
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SIO_000300: 2.549024e6

ClippingRankSum
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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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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.744774400669994e-5
allele num: 57314
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QD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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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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European (Non-Finnish)
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allele num: 57308
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South Asian
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European (Finnish)
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Other
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African
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Latino
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

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

Latino
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South Asian
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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BaseQRankSum
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MQ
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FS
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DP
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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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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Latino
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allele frequency: 2.994609702535436e-4
allele num: 10018
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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South Asian
type: Population
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European (Finnish)
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East Asian
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.618e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.301e0

MQ
type: SiteQuality
SIO_000300: 4.344e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.56e-1

QD
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 2.547957e6

GenotypeQuality
all individuals: 9767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1406
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2928
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.547937e6

MQ
type: SiteQuality
SIO_000300: 4.457e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.517e0

VQSLOD
type: SiteQuality
SIO_000300: -2.443e0

FS
type: SiteQuality
SIO_000300: 7.068e0

MQRankSum
type: SiteQuality
SIO_000300: -1.221e0

QD
type: SiteQuality
SIO_000300: 5.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

GenotypeQuality
all individuals: 9766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 219
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2929
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.537427048972342e-4
allele num: 7882
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14834
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.5e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

DP
type: SiteQuality
SIO_000300: 2.547892e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.89e1

GenotypeQuality
all individuals: 9766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 204
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4462
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.89e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.5e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

DP
type: SiteQuality
SIO_000300: 2.547892e6

GenotypeQuality
all individuals: 2325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9762
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6707
bin: 9.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.493205714884549e-5
allele num: 57254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14832
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 2.548312e6

MQ
type: SiteQuality
SIO_000300: 4.556e1

QD
type: SiteQuality
SIO_000300: 2.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.41e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
all individuals: 3606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6707
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2927
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.742179072276159e-5
allele num: 14832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.41e-2

MQ
type: SiteQuality
SIO_000300: 4.556e1

FS
type: SiteQuality
SIO_000300: 7.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 2.548312e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 2.41e0

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6633
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 22472
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.401198024310786e-4
allele num: 57094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 6.772009029345372e-4
allele num: 4430
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.349527665317139e-4
allele num: 14820
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.01010101010101e-4
allele num: 9900
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.277465508431272e-4
allele num: 7828
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

MQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQ
type: SiteQuality
SIO_000300: 4.334e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.34e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.59e0

DP
type: SiteQuality
SIO_000300: 2.573612e6

GenotypeQuality
all individuals: 6633
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 22472
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9760
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3595
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1403
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 971
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 963
bin: 8.75e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 1.01010101010101e-4
allele num: 9900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.2531328320802e-3
allele num: 798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.90419308508775e-4
allele num: 57094
num of homozygotes: 6

African
type: Population
allele count: 12
allele frequency: 2.708803611738149e-3
allele num: 4430
num of homozygotes: 4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 4.334e1

DP
type: SiteQuality
SIO_000300: 2.573612e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.34e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 3.59e0

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2471
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 2311
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 22472
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1090
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6633
bin: 9.75e1
variant carriers: 335

GenotypeQuality
all individuals: 963
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 1

Other
type: Population
allele count: 7
allele frequency: 8.771929824561403e-3
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 184
allele frequency: 3.222755455914807e-3
allele num: 57094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.92929292929293e-3
allele num: 9900
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 2.031602708803612e-3
allele num: 4430
num of homozygotes: 1

East Asian
type: Population
allele count: 3
allele frequency: 3.832396525293817e-4
allele num: 7828
num of homozygotes: 0

South Asian
type: Population
allele count: 116
allele frequency: 7.827260458839407e-3
allele num: 14820
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

QD
type: SiteQuality
SIO_000300: 3.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.34e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

MQ
type: SiteQuality
SIO_000300: 4.334e1

DP
type: SiteQuality
SIO_000300: 2.573612e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

GenotypeQuality
all individuals: 1003
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 2353
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2335
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 6166
bin: 9.75e1
variant carriers: 1164

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2933
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 6

South Asian
type: Population
allele count: 19
allele frequency: 1.284304447749087e-3
allele num: 14794
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 1.136363636363636e-2
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 4.977375565610859e-3
allele num: 4420
num of homozygotes: 0

Latino
type: Population
allele count: 783
allele frequency: 7.984907199673669e-2
allele num: 9806
num of homozygotes: 0

East Asian
type: Population
allele count: 84
allele frequency: 1.071155317521041e-2
allele num: 7842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 144
allele frequency: 2.519773220410163e-3
allele num: 57148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 157
allele frequency: 2.587343441001978e-2
allele num: 6068
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 2.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -1.193e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.968e0

MQ
type: SiteQuality
SIO_000300: 4.391e1

DP
type: SiteQuality
SIO_000300: 2.55325e6

GenotypeQuality
all individuals: 1417
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2335
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1003
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 959
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6166
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 3632
bin: 7.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.924826765591097e-4
allele num: 57148
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.524886877828054e-4
allele num: 4420
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.35189941868325e-4
allele num: 14794
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.591957811470006e-4
allele num: 6068
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.193e0

MQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.968e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

DP
type: SiteQuality
SIO_000300: 2.55325e6

MQ
type: SiteQuality
SIO_000300: 4.391e1

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 997
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 580
bin: 2.5e0
variant carriers: 2

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

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1092
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2409
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5149
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 3719
bin: 7.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.55307994757536e-4
allele num: 6104
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.49842555105713e-4
allele num: 4446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.398014818957081e-4
allele num: 57224
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.004621257785815e-4
allele num: 9954
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.75310642895732e-5
allele num: 14808
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.187259e6

MQ
type: SiteQuality
SIO_000300: 4.216e1

VQSLOD
type: SiteQuality
SIO_000300: -1.298e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.482e-1

FS
type: SiteQuality
SIO_000300: 1.2627e2

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 9.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 1092
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5149
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 2409
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 23337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10100
bin: 6.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.223262966587446e-4
allele num: 57224
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.269357705001269e-4
allele num: 7878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.004621257785815e-4
allele num: 9954
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 6.747638326585695e-4
allele num: 4446
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.350621285791464e-4
allele num: 14808
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.482e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 2.187259e6

VQSLOD
type: SiteQuality
SIO_000300: -1.298e1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

FS
type: SiteQuality
SIO_000300: 1.2627e2

MQ
type: SiteQuality
SIO_000300: 4.216e1

QD
type: SiteQuality
SIO_000300: 9.99e0

GenotypeQuality
all individuals: 3715
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23366
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5083
bin: 9.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.179455e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 3.528e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: -3.129e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.536e1

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23246
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3704
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3400
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1441
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.751865737009916e-5
allele num: 57082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.272912423625254e-4
allele num: 7856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6088
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 1.781e0

MQ
type: SiteQuality
SIO_000300: 4.358e1

VQSLOD
type: SiteQuality
SIO_000300: -4.095e0

QD
type: SiteQuality
SIO_000300: 3.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.195e0

DP
type: SiteQuality
SIO_000300: 2.174776e6

GenotypeQuality
all individuals: 10067
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23251
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3398
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.757669955399378e-5
allele num: 14798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 2.174551e6

FS
type: SiteQuality
SIO_000300: 5.048e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

MQ
type: SiteQuality
SIO_000300: 4.339e1

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

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23258
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.757669955399378e-5
allele num: 14798
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 6.064281382656155e-4
allele num: 9894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.503977013910789e-5
allele num: 57078
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.272912423625254e-4
allele num: 7856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6086
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.174198e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.087e0

MQ
type: SiteQuality
SIO_000300: 4.369e1

QD
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: -2.246e0

FS
type: SiteQuality
SIO_000300: 2.164e0

MQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2400
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5069
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.75266404935502e-5
allele num: 57056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.170289e6

QD
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

MQ
type: SiteQuality
SIO_000300: 4.233e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

FS
type: SiteQuality
SIO_000300: 9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.847e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 23089
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5067
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 993
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.508402624285163e-5
allele num: 57006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.274534794799898e-4
allele num: 7846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14778
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.734e0

DP
type: SiteQuality
SIO_000300: 2.166885e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.813e0

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

QD
type: SiteQuality
SIO_000300: 7.6e-1

MQ
type: SiteQuality
SIO_000300: 4.266e1

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.755494698406011e-5
allele num: 56964
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.269e1

QD
type: SiteQuality
SIO_000300: 1.626e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.126e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.72e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.046e0

DP
type: SiteQuality
SIO_000300: 2.163112e6

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 3.591e0

GenotypeQuality
all individuals: 1281
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 10006
bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 122
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.53514739229025e-4
allele num: 4410
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6074
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56964
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.126e0

QD
type: SiteQuality
SIO_000300: 1.626e1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.046e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.72e-2

FS
type: SiteQuality
SIO_000300: 3.591e0

MQ
type: SiteQuality
SIO_000300: 4.269e1

DP
type: SiteQuality
SIO_000300: 2.163112e6

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.275510204081633e-4
allele num: 7840
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

MQ
type: SiteQuality
SIO_000300: 4.25e1

MQRankSum
type: SiteQuality
SIO_000300: -9.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.996e0

QD
type: SiteQuality
SIO_000300: 4.2e-1

FS
type: SiteQuality
SIO_000300: 9.256e0

DP
type: SiteQuality
SIO_000300: 2.158986e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

GenotypeQuality
all individuals: 3132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5063
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variant carriers: 10

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.053740779768177e-4
allele num: 56940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.061738424045491e-4
allele num: 9848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.25e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

DP
type: SiteQuality
SIO_000300: 2.158986e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-1

FS
type: SiteQuality
SIO_000300: 9.256e0

MQRankSum
type: SiteQuality
SIO_000300: -9.62e-1

QD
type: SiteQuality
SIO_000300: 4.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.996e0

GenotypeQuality
all individuals: 59
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22613
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 2.276867030965392e-4
allele num: 4392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

VQSLOD
type: SiteQuality
SIO_000300: -3.039e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

FS
type: SiteQuality
SIO_000300: 1.0083e1

DP
type: SiteQuality
SIO_000300: 2.152262e6

MQ
type: SiteQuality
SIO_000300: 4.221e1

QD
type: SiteQuality
SIO_000300: 6.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.758025385886572e-5
allele num: 56882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.221e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 1.0083e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e0

DP
type: SiteQuality
SIO_000300: 2.152262e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

QD
type: SiteQuality
SIO_000300: 6.05e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.27463253393347e-5
allele num: 56876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4388
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14738
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.37e-1

FS
type: SiteQuality
SIO_000300: 2.152e0

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 4.305e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

DP
type: SiteQuality
SIO_000300: 2.150509e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

QD
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: -2.503e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4386
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: 7828
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

QD
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 2.14796e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

MQ
type: SiteQuality
SIO_000300: 5.191e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

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: 3

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 4.593477262287552e-4
allele num: 4354
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.811061163329247e-5
allele num: 14682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56716
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQ
type: SiteQuality
SIO_000300: 4.201e1

FS
type: SiteQuality
SIO_000300: 8.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

DP
type: SiteQuality
SIO_000300: 2.130083e6

VQSLOD
type: SiteQuality
SIO_000300: -2.026e0

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2867
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GenotypeQuality
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GenotypeQuality
all individuals: 2766
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.762797912847271e-5
allele num: 56728
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.299908003679853e-4
allele num: 4348
num of homozygotes: 0

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

VQSLOD
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SIO_000300: -2.859e0

BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: 5.639999999999999e-1

QD
type: SiteQuality
SIO_000300: 8.09e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e0

FS
type: SiteQuality
SIO_000300: 2.93e0

DP
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SIO_000300: 2.131055e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQ
type: SiteQuality
SIO_000300: 4.387e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 1.269035532994924e-3
allele num: 788
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 14684
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 4.084967320261438e-4
allele num: 9792
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4356
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56726
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.79e-1

InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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SIO_000300: 2.8e-2

ReadPosRankSum
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DP
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SIO_000300: 2.130618e6

BaseQRankSum
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SIO_000300: 1.71e0

MQ
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SIO_000300: 4.157e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.815703380588877e-5
allele num: 14672
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9768
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6056
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56668
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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DP
type: SiteQuality
SIO_000300: 2.126069e6

BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 2.35e0

MQ
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SIO_000300: 3.776e1

QD
type: SiteQuality
SIO_000300: 1.85e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

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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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6056
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.764664360838569e-5
allele num: 56668
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.08e0

VQSLOD
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MQ
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SIO_000300: 4.21e1

BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 1.083e1

InbreedingCoeff
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SIO_000300: -4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6050
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

South Asian
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BaseQRankSum
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SIO_000300: -9.64e-1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56596
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7794
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6048
num of homozygotes: 0

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

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

Other
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allele num: 786
num of homozygotes: 0

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

South Asian
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East Asian
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allele num: 7794
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European (Finnish)
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FS
type: SiteQuality
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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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

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.766909322213584e-5
allele num: 56596
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VQSLOD
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MQRankSum
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QD
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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FS
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ReadPosRankSum
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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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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 56596
num of homozygotes: 0

Latino
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South Asian
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African
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European (Finnish)
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East Asian
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 20434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.347402944636555e-5
allele num: 56102
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.235e0

QD
type: SiteQuality
SIO_000300: 1.107e1

MQ
type: SiteQuality
SIO_000300: 4.213e1

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.082626e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.361e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

GenotypeQuality
all individuals: 5013
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19777
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.805575617506861e-5
allele num: 55384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-1

DP
type: SiteQuality
SIO_000300: 2.04043e6

QD
type: SiteQuality
SIO_000300: 4.87e0

VQSLOD
type: SiteQuality
SIO_000300: -4.973e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.757e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.44e-1

FS
type: SiteQuality
SIO_000300: 1.6767e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

MQ
type: SiteQuality
SIO_000300: 3.817e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5011
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1409
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.80583646344987e-5
allele num: 55376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.111e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: -3.775e0

MQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.126e0

FS
type: SiteQuality
SIO_000300: 6.268e0

QD
type: SiteQuality
SIO_000300: 2.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.853e0

DP
type: SiteQuality
SIO_000300: 2.039045e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7749
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3996
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.190580503833516e-4
allele num: 9130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5842
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

DP
type: SiteQuality
SIO_000300: 1.972331e6

MQ
type: SiteQuality
SIO_000300: 4.133e1

VQSLOD
type: SiteQuality
SIO_000300: -3.974e0

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e0

FS
type: SiteQuality
SIO_000300: 1.261e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7658
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3088
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.673080140538732e-4
allele num: 11954
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47182
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 3.555e1

MQRankSum
type: SiteQuality
SIO_000300: -7.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.351e0

VQSLOD
type: SiteQuality
SIO_000300: -3.508e0

FS
type: SiteQuality
SIO_000300: 1.306e0

DP
type: SiteQuality
SIO_000300: 1.486773e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

GenotypeQuality
all individuals: 2212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7424
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.58663918942126e-5
allele num: 11646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45694
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.462e0

VQSLOD
type: SiteQuality
SIO_000300: -2.186e0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.73e-1

MQ
type: SiteQuality
SIO_000300: 4.24e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.369304e6