14-51239765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239765
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239765
    reference: chr 14
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.715G>A
  hgvsp: ENSP00000374518.3:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.715G>A
  hgvsp: ENSP00000412391.1:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.715G>A
  hgvsp: ENSP00000436092.2:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.601G>A
  hgvsp: ENSP00000398641.2:p.Val201Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.715G>A
  hgvsp: ENSP00000371472.3:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.715G>A
  hgvsp: ENSP00000245441.5:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.715G>A
  hgvsp: ENSP00000432924.1:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.715G>A
  hgvsp: ENSP00000371474.4:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.715G>A
  hgvsp: ENSP00000324210.9:p.Val239Ile
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val239Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

14-51239768-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239768
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239768
    reference: chr 14
allele count: 2
allele frequency: 1.650655310158133e-5
allele num: 121164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.712A>C
  hgvsp: ENSP00000432924.1:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.712A>C
  hgvsp: ENSP00000245441.5:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.712A>C
  hgvsp: ENSP00000412391.1:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.712A>C
  hgvsp: ENSP00000371472.3:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.712A>C
  hgvsp: ENSP00000324210.9:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.598A>C
  hgvsp: ENSP00000398641.2:p.Ser200Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.712A>C
  hgvsp: ENSP00000436092.2:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.712A>C
  hgvsp: ENSP00000371474.4:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.712A>C
  hgvsp: ENSP00000374518.3:p.Ser238Arg
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser238Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-51239777-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239777
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239777
    reference: chr 14
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.703G>A
  hgvsp: ENSP00000374518.3:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.703G>A
  hgvsp: ENSP00000371472.3:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.589G>A
  hgvsp: ENSP00000398641.2:p.Gly197Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.703G>A
  hgvsp: ENSP00000245441.5:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.703G>A
  hgvsp: ENSP00000412391.1:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.703G>A
  hgvsp: ENSP00000371474.4:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.703G>A
  hgvsp: ENSP00000324210.9:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.703G>A
  hgvsp: ENSP00000436092.2:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.703G>A
  hgvsp: ENSP00000432924.1:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly235Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-51239778-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239778
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239778
    reference: chr 14
allele count: 20
allele frequency: 1.650818806127839e-4
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.702C>T
  hgvsp: ENST00000245441.5:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.702C>T
  hgvsp: ENST00000389868.3:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.702C>T
  hgvsp: ENST00000382043.4:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.702C>T
  hgvsp: ENST00000530997.2:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.702C>T
  hgvsp: ENST00000324330.9:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.702C>T
  hgvsp: ENST00000476352.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.702C>T
  hgvsp: ENST00000382041.3:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.702C>T
  hgvsp: ENST00000453196.1:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.588C>T
  hgvsp: ENST00000453401.2:c.588C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19464
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4391
  bin: 9.75e1
  variant carriers: 20
hgvs: p.Asp234Asp
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

14-51239783-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239783
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239783
    reference: chr 14
allele count: 1
allele frequency: 8.255456856982466e-6
allele num: 121132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.697C>A
  hgvsp: ENSP00000432924.1:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.697C>A
  hgvsp: ENSP00000245441.5:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.697C>A
  hgvsp: ENSP00000371472.3:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.697C>A
  hgvsp: ENSP00000324210.9:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.583C>A
  hgvsp: ENSP00000398641.2:p.Pro195Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.697C>A
  hgvsp: ENSP00000412391.1:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.697C>A
  hgvsp: ENSP00000371474.4:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.697C>A
  hgvsp: ENSP00000436092.2:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.697C>A
  hgvsp: ENSP00000374518.3:p.Pro233Thr
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro233Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS

14-51239785-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239785
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239785
    reference: chr 14
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.695A>T
  hgvsp: ENSP00000371474.4:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.695A>T
  hgvsp: ENSP00000432924.1:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.695A>T
  hgvsp: ENSP00000436092.2:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.695A>T
  hgvsp: ENSP00000374518.3:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.695A>T
  hgvsp: ENSP00000245441.5:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.695A>T
  hgvsp: ENSP00000371472.3:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.695A>T
  hgvsp: ENSP00000412391.1:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.581A>T
  hgvsp: ENSP00000398641.2:p.Asp194Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.695A>T
  hgvsp: ENSP00000324210.9:p.Asp232Val
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6897
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp232Val
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

14-51239802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239802
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239802
    reference: chr 14
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.678A>G
  hgvsp: ENST00000382043.4:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.564A>G
  hgvsp: ENST00000453401.2:c.564A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.678A>G
  hgvsp: ENST00000382041.3:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.678A>G
  hgvsp: ENST00000453196.1:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.678A>G
  hgvsp: ENST00000245441.5:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.678A>G
  hgvsp: ENST00000476352.1:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.678A>G
  hgvsp: ENST00000324330.9:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.678A>G
  hgvsp: ENST00000389868.3:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.678A>G
  hgvsp: ENST00000530997.2:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu226Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

14-51239807-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239807
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239807
    reference: chr 14
allele count: 17
allele frequency: 1.409221280899249e-4
allele num: 120634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.673G>A
  hgvsp: ENSP00000245441.5:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.673G>A
  hgvsp: ENSP00000371474.4:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.673G>A
  hgvsp: ENSP00000412391.1:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.673G>A
  hgvsp: ENSP00000374518.3:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.673G>A
  hgvsp: ENSP00000432924.1:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.673G>A
  hgvsp: ENSP00000436092.2:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.559G>A
  hgvsp: ENSP00000398641.2:p.Glu187Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.673G>A
  hgvsp: ENSP00000324210.9:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.673G>A
  hgvsp: ENSP00000371472.3:p.Glu225Lys
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19385
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu225Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

14-51239808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239808
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239808
    reference: chr 14
allele count: 2
allele frequency: 1.659090154959021e-5
allele num: 120548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.672C>T
  hgvsp: ENST00000324330.9:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.672C>T
  hgvsp: ENST00000382041.3:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.672C>T
  hgvsp: ENST00000382043.4:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.672C>T
  hgvsp: ENST00000245441.5:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.672C>T
  hgvsp: ENST00000530997.2:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.672C>T
  hgvsp: ENST00000476352.1:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.672C>T
  hgvsp: ENST00000453196.1:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.672C>T
  hgvsp: ENST00000389868.3:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.558C>T
  hgvsp: ENST00000453401.2:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu224Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

14-51239809-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239809
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239809
    reference: chr 14
allele count: 3
allele frequency: 2.489089491064169e-5
allele num: 120526
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.671T>C
  hgvsp: ENSP00000374518.3:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.671T>C
  hgvsp: ENSP00000324210.9:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.671T>C
  hgvsp: ENSP00000412391.1:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.671T>C
  hgvsp: ENSP00000245441.5:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.557T>C
  hgvsp: ENSP00000398641.2:p.Leu186Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.671T>C
  hgvsp: ENSP00000371472.3:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.671T>C
  hgvsp: ENSP00000436092.2:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.671T>C
  hgvsp: ENSP00000371474.4:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.671T>C
  hgvsp: ENSP00000432924.1:p.Leu224Pro
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu224Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

14-51239810-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239810
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239810
    reference: chr 14
allele count: 1
allele frequency: 8.296964970213896e-6
allele num: 120526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.670C>T
  hgvsp: ENSP00000432924.1:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.556C>T
  hgvsp: ENSP00000398641.2:p.Leu186Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.670C>T
  hgvsp: ENSP00000245441.5:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.670C>T
  hgvsp: ENSP00000436092.2:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.670C>T
  hgvsp: ENSP00000374518.3:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.670C>T
  hgvsp: ENSP00000324210.9:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.670C>T
  hgvsp: ENSP00000371472.3:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.670C>T
  hgvsp: ENSP00000371474.4:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.670C>T
  hgvsp: ENSP00000412391.1:p.Leu224Phe
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40592
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu224Phe
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

14-51239826-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239826
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239826
    reference: chr 14
allele count: 1
allele frequency: 8.358688020328329e-6
allele num: 119636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-13G>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

14-51239829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239829
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239829
    reference: chr 14
allele count: 4
allele frequency: 3.34941050375134e-5
allele num: 119424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-16G>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36721
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

14-51239842-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239842
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239842
    reference: chr 14
allele count: 3
allele frequency: 2.523935319950867e-5
allele num: 118862
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-29A>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15546
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30857
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

14-51239848-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239848
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239848
    reference: chr 14
allele count: 1
allele frequency: 8.442523301364311e-6
allele num: 118448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-35T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-35T>C
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13707
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3776
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3801
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

14-51239855-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239855
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239855
    reference: chr 14
allele count: 7
allele frequency: 5.941165486920948e-5
allele num: 117822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-42A>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18578
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11622
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4355
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21170
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

14-51239857-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239857
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239857
    reference: chr 14
allele count: 1
allele frequency: 8.505281779985371e-6
allele num: 117574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-44A>T
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5098
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3744
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

14-51239859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239859
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239859
    reference: chr 14
allele count: 7
allele frequency: 5.97137153873714e-5
allele num: 117226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-46G>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12009
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19755
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5247
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2037
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2398
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-51239860-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239860
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239860
    reference: chr 14
allele count: 1
allele frequency: 8.547739123001965e-6
allele num: 116990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-47T>C
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2023
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4350
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3001
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3593
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/14-51239861-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239861
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239861
    reference: chr 14
allele count: 6
allele frequency: 5.134876078323976e-5
allele num: 116848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-48T>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20055
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10138
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4354
  bin: 9.75e1
  variant carriers: 6
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP

14-51239862-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239862
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239862
    reference: chr 14
allele count: 1
allele frequency: 8.544379507160189e-6
allele num: 117036
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-49C>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20257
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

14-51239863-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51239863
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51239863
    reference: chr 14
allele count: 1
allele frequency: 8.557980316645272e-6
allele num: 116850
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.553-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.667-50C>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11922
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3489
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 5.75e1
  variant carriers: 0
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: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

14-51243619-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243619
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243619
    reference: chr 14
allele count: 1
allele frequency: 8.842045695692155e-6
allele num: 113096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+48A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+48A>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15959
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-51243628-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243628
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243627
    reference: chr 14
allele count: 1
allele frequency: 8.832985902554499e-6
allele num: 113212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+38delG
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: AC
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/14-51243629-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243629
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243630
    reference: chr 14
allele count: 5
allele frequency: 4.416336913510458e-5
allele num: 113216
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+37_552+38insT
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+37_666+38insT
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/14-51243639-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243639
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243639
    reference: chr 14
allele count: 2
allele frequency: 1.761183515322297e-5
allele num: 113560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+28G>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+28G>T
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12822
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3049
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6354
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-51243655-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243655
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243655
    reference: chr 14
allele count: 1
allele frequency: 8.708222303498963e-6
allele num: 114834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+12A>C
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6376
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4911
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-51243657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243657
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243657
    reference: chr 14
allele count: 4
allele frequency: 3.477353733808572e-5
allele num: 115030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+10G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+10G>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6377
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4911
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

14-51243665-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243665
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243665
    reference: chr 14
allele count: 1
allele frequency: 8.557540905045526e-6
allele num: 116856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.552+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.666+2T>C
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
hgvs: c.666+2T>C
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: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

14-51243673-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243673
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243673
    reference: chr 14
allele count: 1
allele frequency: 8.461811843151855e-6
allele num: 118178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.660T>C
  hgvsp: ENST00000382043.4:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.660T>C
  hgvsp: ENST00000389868.3:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.660T>C
  hgvsp: ENST00000453196.1:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.660T>C
  hgvsp: ENST00000476352.1:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.660T>C
  hgvsp: ENST00000245441.5:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.546T>C
  hgvsp: ENST00000453401.2:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.660T>C
  hgvsp: ENST00000382041.3:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.660T>C
  hgvsp: ENST00000530997.2:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.660T>C
  hgvsp: ENST00000324330.9:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp220Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

14-51243703-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243703
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243703
    reference: chr 14
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.630C>G
  hgvsp: ENSP00000245441.5:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.630C>G
  hgvsp: ENSP00000412391.1:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.630C>G
  hgvsp: ENSP00000374518.3:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.630C>G
  hgvsp: ENSP00000371474.4:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.516C>G
  hgvsp: ENSP00000398641.2:p.Ile172Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.630C>G
  hgvsp: ENSP00000432924.1:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.630C>G
  hgvsp: ENSP00000436092.2:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.630C>G
  hgvsp: ENSP00000371472.3:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.630C>G
  hgvsp: ENSP00000324210.9:p.Ile210Met
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile210Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-51243711-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243711
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243711
    reference: chr 14
allele count: 2
allele frequency: 1.651473114017704e-5
allele num: 121104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.622G>T
  hgvsp: ENSP00000371474.4:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.622G>T
  hgvsp: ENSP00000245441.5:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.508G>T
  hgvsp: ENSP00000398641.2:p.Val170Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.622G>T
  hgvsp: ENSP00000324210.9:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.622G>T
  hgvsp: ENSP00000371472.3:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.622G>T
  hgvsp: ENSP00000436092.2:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.622G>T
  hgvsp: ENSP00000374518.3:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.622G>T
  hgvsp: ENSP00000432924.1:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.622G>T
  hgvsp: ENSP00000412391.1:p.Val208Phe
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val208Phe
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

14-51243714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243714
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243714
    reference: chr 14
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.619C>T
  hgvsp: ENST00000453196.1:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.619C>T
  hgvsp: ENST00000245441.5:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.505C>T
  hgvsp: ENST00000453401.2:c.505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.619C>T
  hgvsp: ENST00000382043.4:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.619C>T
  hgvsp: ENST00000476352.1:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.619C>T
  hgvsp: ENST00000324330.9:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.619C>T
  hgvsp: ENST00000389868.3:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.619C>T
  hgvsp: ENST00000530997.2:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.619C>T
  hgvsp: ENST00000382041.3:c.619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4169
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu207Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

14-51243718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243718
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243718
    reference: chr 14
allele count: 4
allele frequency: 3.299948850792813e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.615G>A
  hgvsp: ENST00000476352.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.615G>A
  hgvsp: ENST00000530997.2:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.615G>A
  hgvsp: ENST00000382043.4:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.501G>A
  hgvsp: ENST00000453401.2:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.615G>A
  hgvsp: ENST00000453196.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.615G>A
  hgvsp: ENST00000382041.3:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.615G>A
  hgvsp: ENST00000245441.5:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.615G>A
  hgvsp: ENST00000324330.9:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.615G>A
  hgvsp: ENST00000389868.3:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12956
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4941
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys205Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

14-51243721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243721
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243721
    reference: chr 14
allele count: 76
allele frequency: 6.267937848447861e-4
allele num: 121252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.612G>A
  hgvsp: ENST00000476352.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.612G>A
  hgvsp: ENST00000453196.1:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.612G>A
  hgvsp: ENST00000324330.9:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.612G>A
  hgvsp: ENST00000389868.3:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.612G>A
  hgvsp: ENST00000530997.2:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.612G>A
  hgvsp: ENST00000245441.5:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.498G>A
  hgvsp: ENST00000453401.2:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.612G>A
  hgvsp: ENST00000382041.3:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.612G>A
  hgvsp: ENST00000382043.4:c.612G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8550
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 9.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6693
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg204Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-51243722-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243722
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243722
    reference: chr 14
allele count: 4
allele frequency: 3.298805832288711e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.611G>A
  hgvsp: ENSP00000371474.4:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.611G>A
  hgvsp: ENSP00000412391.1:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.611G>A
  hgvsp: ENSP00000371472.3:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.611G>A
  hgvsp: ENSP00000245441.5:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.497G>A
  hgvsp: ENSP00000398641.2:p.Arg166Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.611G>A
  hgvsp: ENSP00000436092.2:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.611G>A
  hgvsp: ENSP00000432924.1:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.611G>A
  hgvsp: ENSP00000374518.3:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.611G>A
  hgvsp: ENSP00000324210.9:p.Arg204Gln
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg204Gln
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ

14-51243723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243723
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243723
    reference: chr 14
allele count: 2
allele frequency: 1.649266900862567e-5
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.610C>T
  hgvsp: ENSP00000245441.5:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.610C>T
  hgvsp: ENSP00000371474.4:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.610C>T
  hgvsp: ENSP00000432924.1:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.610C>T
  hgvsp: ENSP00000412391.1:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.496C>T
  hgvsp: ENSP00000398641.2:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.610C>T
  hgvsp: ENSP00000436092.2:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.610C>T
  hgvsp: ENSP00000324210.9:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.610C>T
  hgvsp: ENSP00000374518.3:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.610C>T
  hgvsp: ENSP00000371472.3:p.Arg204Trp
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20603
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg204Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

14-51243724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243724
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243724
    reference: chr 14
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.609C>T
  hgvsp: ENST00000324330.9:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.609C>T
  hgvsp: ENST00000476352.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.609C>T
  hgvsp: ENST00000453196.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.609C>T
  hgvsp: ENST00000382043.4:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.609C>T
  hgvsp: ENST00000245441.5:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.609C>T
  hgvsp: ENST00000530997.2:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.609C>T
  hgvsp: ENST00000389868.3:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.609C>T
  hgvsp: ENST00000382041.3:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.495C>T
  hgvsp: ENST00000453401.2:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4945
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn203Asn
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

14-51243728-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243728
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243728
    reference: chr 14
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.491T>C
  hgvsp: ENSP00000398641.2:p.Leu164Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.605T>C
  hgvsp: ENSP00000324210.9:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.605T>C
  hgvsp: ENSP00000371472.3:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.605T>C
  hgvsp: ENSP00000374518.3:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.605T>C
  hgvsp: ENSP00000436092.2:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.605T>C
  hgvsp: ENSP00000245441.5:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.605T>C
  hgvsp: ENSP00000412391.1:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.605T>C
  hgvsp: ENSP00000371474.4:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.605T>C
  hgvsp: ENSP00000432924.1:p.Leu202Pro
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu202Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

14-51243733-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243733
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243733
    reference: chr 14
allele count: 353
allele frequency: 2.909900255543648e-3
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.600T>C
  hgvsp: ENST00000530997.2:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.486T>C
  hgvsp: ENST00000453401.2:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.600T>C
  hgvsp: ENST00000476352.1:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.600T>C
  hgvsp: ENST00000245441.5:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.600T>C
  hgvsp: ENST00000324330.9:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.600T>C
  hgvsp: ENST00000382043.4:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.600T>C
  hgvsp: ENST00000389868.3:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.600T>C
  hgvsp: ENST00000382041.3:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  clinical significance: likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.600T>C
  hgvsp: ENST00000453196.1:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 8541
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 12955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 9.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly200Gly
num of homozygotes: 5
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

14-51243736-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243736
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243736
    reference: chr 14
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.597T>A
  hgvsp: ENSP00000412391.1:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.597T>A
  hgvsp: ENSP00000245441.5:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.597T>A
  hgvsp: ENSP00000432924.1:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.597T>A
  hgvsp: ENSP00000371472.3:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.597T>A
  hgvsp: ENSP00000436092.2:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.597T>A
  hgvsp: ENSP00000374518.3:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.483T>A
  hgvsp: ENSP00000398641.2:p.Asp161Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.597T>A
  hgvsp: ENSP00000371474.4:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.597T>A
  hgvsp: ENSP00000324210.9:p.Asp199Glu
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp199Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

14-51243740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243740
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243740
    reference: chr 14
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.593G>A
  hgvsp: ENSP00000371472.3:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.593G>A
  hgvsp: ENSP00000245441.5:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.593G>A
  hgvsp: ENSP00000374518.3:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.479G>A
  hgvsp: ENSP00000398641.2:p.Arg160His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.593G>A
  hgvsp: ENSP00000324210.9:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.593G>A
  hgvsp: ENSP00000436092.2:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.593G>A
  hgvsp: ENSP00000432924.1:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.593G>A
  hgvsp: ENSP00000371474.4:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.593G>A
  hgvsp: ENSP00000412391.1:p.Arg198His
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg198His
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

14-51243743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243743
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243743
    reference: chr 14
allele count: 4
allele frequency: 3.29663084327817e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.590C>T
  hgvsp: ENSP00000436092.2:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.590C>T
  hgvsp: ENSP00000245441.5:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.590C>T
  hgvsp: ENSP00000371472.3:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.590C>T
  hgvsp: ENSP00000432924.1:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.590C>T
  hgvsp: ENSP00000371474.4:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.590C>T
  hgvsp: ENSP00000324210.9:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.590C>T
  hgvsp: ENSP00000412391.1:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.590C>T
  hgvsp: ENSP00000374518.3:p.Thr197Ile
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.476C>T
  hgvsp: ENSP00000398641.2:p.Thr159Ile
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14938
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4959
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr197Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-51243747-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243747
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243747
    reference: chr 14
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.586A>G
  hgvsp: ENSP00000374518.3:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.586A>G
  hgvsp: ENSP00000371472.3:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.586A>G
  hgvsp: ENSP00000432924.1:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.586A>G
  hgvsp: ENSP00000245441.5:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.586A>G
  hgvsp: ENSP00000412391.1:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.586A>G
  hgvsp: ENSP00000436092.2:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.472A>G
  hgvsp: ENSP00000398641.2:p.Ile158Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.586A>G
  hgvsp: ENSP00000324210.9:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.586A>G
  hgvsp: ENSP00000371474.4:p.Ile196Val
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile196Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-51243754-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243754
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243754
    reference: chr 14
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.579T>G
  hgvsp: ENSP00000371474.4:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.579T>G
  hgvsp: ENSP00000436092.2:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.579T>G
  hgvsp: ENSP00000374518.3:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.579T>G
  hgvsp: ENSP00000432924.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.579T>G
  hgvsp: ENSP00000371472.3:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.465T>G
  hgvsp: ENSP00000398641.2:p.Asp155Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.579T>G
  hgvsp: ENSP00000245441.5:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.579T>G
  hgvsp: ENSP00000324210.9:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.579T>G
  hgvsp: ENSP00000412391.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp193Glu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

14-51243765-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243765
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243765
    reference: chr 14
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.454G>C
  hgvsp: ENSP00000398641.2:p.Val152Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.568G>C
  hgvsp: ENSP00000436092.2:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.568G>C
  hgvsp: ENSP00000412391.1:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.568G>C
  hgvsp: ENSP00000371472.3:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.568G>C
  hgvsp: ENSP00000324210.9:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.568G>C
  hgvsp: ENSP00000245441.5:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.568G>C
  hgvsp: ENSP00000432924.1:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.568G>C
  hgvsp: ENSP00000371474.4:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.568G>C
  hgvsp: ENSP00000374518.3:p.Val190Leu
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val190Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

14-51243766-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243766
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243766
    reference: chr 14
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.567A>G
  hgvsp: ENST00000453196.1:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.567A>G
  hgvsp: ENST00000382041.3:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.453A>G
  hgvsp: ENST00000453401.2:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.567A>G
  hgvsp: ENST00000530997.2:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.567A>G
  hgvsp: ENST00000476352.1:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.567A>G
  hgvsp: ENST00000382043.4:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.567A>G
  hgvsp: ENST00000245441.5:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.567A>G
  hgvsp: ENST00000324330.9:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.567A>G
  hgvsp: ENST00000389868.3:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu189Glu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

14-51243771-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243771
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243771
    reference: chr 14
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.562C>G
  hgvsp: ENSP00000432924.1:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.562C>G
  hgvsp: ENSP00000371472.3:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.562C>G
  hgvsp: ENSP00000412391.1:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.562C>G
  hgvsp: ENSP00000436092.2:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.448C>G
  hgvsp: ENSP00000398641.2:p.Gln150Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.562C>G
  hgvsp: ENSP00000245441.5:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.562C>G
  hgvsp: ENSP00000374518.3:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.562C>G
  hgvsp: ENSP00000371474.4:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.562C>G
  hgvsp: ENSP00000324210.9:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln188Glu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

14-51243785-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243785
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243785
    reference: chr 14
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.548T>C
  hgvsp: ENSP00000324210.9:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.548T>C
  hgvsp: ENSP00000412391.1:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.548T>C
  hgvsp: ENSP00000374518.3:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.548T>C
  hgvsp: ENSP00000245441.5:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.548T>C
  hgvsp: ENSP00000371474.4:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.548T>C
  hgvsp: ENSP00000436092.2:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.548T>C
  hgvsp: ENSP00000432924.1:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.434T>C
  hgvsp: ENSP00000398641.2:p.Ile145Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.548T>C
  hgvsp: ENSP00000371472.3:p.Ile183Thr
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4955
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile183Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-51243787-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243787
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243787
    reference: chr 14
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.546G>T
  hgvsp: ENSP00000374518.3:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.546G>T
  hgvsp: ENSP00000245441.5:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.546G>T
  hgvsp: ENSP00000371474.4:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.432G>T
  hgvsp: ENSP00000398641.2:p.Trp144Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.546G>T
  hgvsp: ENSP00000436092.2:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.546G>T
  hgvsp: ENSP00000371472.3:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.546G>T
  hgvsp: ENSP00000324210.9:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.546G>T
  hgvsp: ENSP00000432924.1:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.546G>T
  hgvsp: ENSP00000412391.1:p.Trp182Cys
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Trp182Cys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

14-51243789-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243789
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243789
    reference: chr 14
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.544T>C
  hgvsp: ENSP00000371472.3:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.544T>C
  hgvsp: ENSP00000436092.2:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.544T>C
  hgvsp: ENSP00000324210.9:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.544T>C
  hgvsp: ENSP00000245441.5:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.544T>C
  hgvsp: ENSP00000371474.4:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.430T>C
  hgvsp: ENSP00000398641.2:p.Trp144Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.544T>C
  hgvsp: ENSP00000432924.1:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.544T>C
  hgvsp: ENSP00000412391.1:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.544T>C
  hgvsp: ENSP00000374518.3:p.Trp182Arg
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Trp182Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-51243794-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243794
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243794
    reference: chr 14
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.539A>G
  hgvsp: ENSP00000436092.2:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.539A>G
  hgvsp: ENSP00000371474.4:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.425A>G
  hgvsp: ENSP00000398641.2:p.Gln142Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.539A>G
  hgvsp: ENSP00000412391.1:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.539A>G
  hgvsp: ENSP00000432924.1:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.539A>G
  hgvsp: ENSP00000324210.9:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.539A>G
  hgvsp: ENSP00000371472.3:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.539A>G
  hgvsp: ENSP00000245441.5:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.539A>G
  hgvsp: ENSP00000374518.3:p.Gln180Arg
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln180Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

14-51243800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243800
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243800
    reference: chr 14
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.533C>T
  hgvsp: ENSP00000245441.5:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.419C>T
  hgvsp: ENSP00000398641.2:p.Pro140Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.533C>T
  hgvsp: ENSP00000412391.1:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.533C>T
  hgvsp: ENSP00000371474.4:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.533C>T
  hgvsp: ENSP00000371472.3:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.533C>T
  hgvsp: ENSP00000374518.3:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.533C>T
  hgvsp: ENSP00000324210.9:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.533C>T
  hgvsp: ENSP00000436092.2:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.533C>T
  hgvsp: ENSP00000432924.1:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15720
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro178Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

14-51243805-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243805
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243805
    reference: chr 14
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.528T>C
  hgvsp: ENST00000389868.3:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.414T>C
  hgvsp: ENST00000453401.2:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.528T>C
  hgvsp: ENST00000382043.4:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.528T>C
  hgvsp: ENST00000453196.1:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.528T>C
  hgvsp: ENST00000476352.1:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.528T>C
  hgvsp: ENST00000530997.2:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.528T>C
  hgvsp: ENST00000245441.5:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.528T>C
  hgvsp: ENST00000382041.3:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.528T>C
  hgvsp: ENST00000324330.9:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3284
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser176Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

14-51243808-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243808
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243808
    reference: chr 14
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.525A>C
  hgvsp: ENST00000245441.5:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.525A>C
  hgvsp: ENST00000389868.3:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.411A>C
  hgvsp: ENST00000453401.2:c.411A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.525A>C
  hgvsp: ENST00000530997.2:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.525A>C
  hgvsp: ENST00000382041.3:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.525A>C
  hgvsp: ENST00000382043.4:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.525A>C
  hgvsp: ENST00000453196.1:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.525A>C
  hgvsp: ENST00000324330.9:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.525A>C
  hgvsp: ENST00000476352.1:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4170
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly175Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-51243812-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243812
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243812
    reference: chr 14
allele count: 1
allele frequency: 8.315593400745077e-6
allele num: 120256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.521G>C
  hgvsp: ENSP00000412391.1:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.521G>C
  hgvsp: ENSP00000371472.3:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.521G>C
  hgvsp: ENSP00000245441.5:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.521G>C
  hgvsp: ENSP00000324210.9:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.521G>C
  hgvsp: ENSP00000432924.1:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.521G>C
  hgvsp: ENSP00000371474.4:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.521G>C
  hgvsp: ENSP00000436092.2:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.521G>C
  hgvsp: ENSP00000374518.3:p.Ser174Thr
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.407G>C
  hgvsp: ENSP00000398641.2:p.Ser136Thr
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser174Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/14-51243822-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243822
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243822
    reference: chr 14
allele count: 1
allele frequency: 8.371283150281276e-6
allele num: 119456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.511G>T
  hgvsp: ENSP00000374518.3:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.511G>T
  hgvsp: ENSP00000371472.3:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.511G>T
  hgvsp: ENSP00000436092.2:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.511G>T
  hgvsp: ENSP00000371474.4:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.397G>T
  hgvsp: ENSP00000398641.2:p.Ala133Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.511G>T
  hgvsp: ENSP00000412391.1:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.511G>T
  hgvsp: ENSP00000245441.5:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.511G>T
  hgvsp: ENSP00000432924.1:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.511G>T
  hgvsp: ENSP00000324210.9:p.Ala171Ser
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18393
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala171Ser
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

14-51243824-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243824
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243824
    reference: chr 14
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.509A>G
  hgvsp: ENSP00000371472.3:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.509A>G
  hgvsp: ENSP00000245441.5:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.509A>G
  hgvsp: ENSP00000374518.3:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.509A>G
  hgvsp: ENSP00000371474.4:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.509A>G
  hgvsp: ENSP00000436092.2:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.509A>G
  hgvsp: ENSP00000324210.9:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.395A>G
  hgvsp: ENSP00000398641.2:p.Asn132Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.509A>G
  hgvsp: ENSP00000432924.1:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.509A>G
  hgvsp: ENSP00000412391.1:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn170Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

14-51243835-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243835
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243835
    reference: chr 14
allele count: 1
allele frequency: 8.429997302400863e-6
allele num: 118624
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.498A>G
  hgvsp: ENST00000382041.3:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.498A>G
  hgvsp: ENST00000530997.2:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.498A>G
  hgvsp: ENST00000324330.9:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.498A>G
  hgvsp: ENST00000245441.5:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.498A>G
  hgvsp: ENST00000476352.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.498A>G
  hgvsp: ENST00000382043.4:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.498A>G
  hgvsp: ENST00000453196.1:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.498A>G
  hgvsp: ENST00000389868.3:c.498A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.384A>G
  hgvsp: ENST00000453401.2:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro166Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

14-51243841-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243841
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243841
    reference: chr 14
allele count: 1
allele frequency: 8.464247020585048e-6
allele num: 118144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.492G>C
  hgvsp: ENSP00000436092.2:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.492G>C
  hgvsp: ENSP00000324210.9:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.492G>C
  hgvsp: ENSP00000245441.5:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.492G>C
  hgvsp: ENSP00000432924.1:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.492G>C
  hgvsp: ENSP00000371472.3:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.492G>C
  hgvsp: ENSP00000371474.4:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.378G>C
  hgvsp: ENSP00000398641.2:p.Trp126Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.492G>C
  hgvsp: ENSP00000374518.3:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.492G>C
  hgvsp: ENSP00000412391.1:p.Trp164Cys
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Trp164Cys
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

14-51243869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243869
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243869
    reference: chr 14
allele count: 1
allele frequency: 8.679500755116566e-6
allele num: 115214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-12C>T
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8511
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6175
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15709
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4133
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

14-51243871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243871
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243871
    reference: chr 14
allele count: 1
allele frequency: 8.680706262261498e-6
allele num: 115198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-14T>C
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

14-51243872-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243872
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243872
    reference: chr 14
allele count: 3
allele frequency: 2.609240189256888e-5
allele num: 114976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-15A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-15A>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2855
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

14-51243875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243875
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243875
    reference: chr 14
allele count: 1
allele frequency: 8.73576071004263e-6
allele num: 114472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-18C>T
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4133
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15704
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

14-51243881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243881
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243881
    reference: chr 14
allele count: 2
allele frequency: 1.758953071132062e-5
allele num: 113704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-24G>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-24G>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14526
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4120
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

14-51243882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243882
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243882
    reference: chr 14
allele count: 2
allele frequency: 1.763668430335097e-5
allele num: 113400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-25C>T
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4812
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

14-51243889-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243889
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243889
    reference: chr 14
allele count: 1
allele frequency: 8.853318223670232e-6
allele num: 112952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-32T>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2776
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

14-51243892-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243892
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243892
    reference: chr 14
allele count: 2
allele frequency: 1.774969381778164e-5
allele num: 112678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-35C>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4070
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-51243892-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243892
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243892
    reference: chr 14
allele count: 1
allele frequency: 8.874846908890822e-6
allele num: 112678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-35C>A
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-35C>A
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

14-51243896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51243896
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 51243896
    reference: chr 14
allele count: 9
allele frequency: 8.015532320407545e-5
allele num: 112282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000374518
  ensembl transcript: ENST00000389868
  gene symbol: NIN
  hgvsc: ENST00000389868.3:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000245441
  ensembl transcript: ENST00000245441
  gene symbol: NIN
  hgvsc: ENST00000245441.5:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000436092
  ensembl transcript: ENST00000530997
  gene symbol: NIN
  hgvsc: ENST00000530997.2:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371474
  ensembl transcript: ENST00000382043
  gene symbol: NIN
  hgvsc: ENST00000382043.4:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000371472
  ensembl transcript: ENST00000382041
  gene symbol: NIN
  hgvsc: ENST00000382041.3:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000324210
  ensembl transcript: ENST00000324330
  gene symbol: NIN
  hgvsc: ENST00000324330.9:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000432924
  ensembl transcript: ENST00000476352
  gene symbol: NIN
  hgvsc: ENST00000476352.1:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000398641
  ensembl transcript: ENST00000453401
  gene symbol: NIN
  hgvsc: ENST00000453401.2:c.362-39A>G
  variant of: http://identifiers.org/hgnc/14906
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100503
  ensembl protein: ENSP00000412391
  ensembl transcript: ENST00000453196
  gene symbol: NIN
  hgvsc: ENST00000453196.1:c.476-39A>G
  variant of: http://identifiers.org/hgnc/14906
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11341
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 193
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 603
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6896
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

FS
type: SiteQuality
SIO_000300: 1.0368e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.114e0

QD
type: SiteQuality
SIO_000300: 7.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.268e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: -2.053e0

DP
type: SiteQuality
SIO_000300: 1.682627e6

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

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

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4385
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 6902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41391
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1523
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 195
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31696014828545e-4
allele num: 8632
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

FS
type: SiteQuality
SIO_000300: 1.1037e1

DP
type: SiteQuality
SIO_000300: 1.68249e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

QD
type: SiteQuality
SIO_000300: 1.062e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.955000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6882
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4380
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.506e0

QD
type: SiteQuality
SIO_000300: 1.159e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

FS
type: SiteQuality
SIO_000300: 2.134e0

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

DP
type: SiteQuality
SIO_000300: 1.683356e6

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1517
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2366
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.897430944562488e-4
allele num: 10354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 11
allele frequency: 1.274328081556997e-3
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.505478999669759e-5
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

DP
type: SiteQuality
SIO_000300: 1.683569e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

QD
type: SiteQuality
SIO_000300: 1.224e1

FS
type: SiteQuality
SIO_000300: 5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

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

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 749
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.394e0

VQSLOD
type: SiteQuality
SIO_000300: -1.117e0

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.314e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.682656e6

QD
type: SiteQuality
SIO_000300: 1.624e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41526
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 256
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4371
bin: 9.75e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

QD
type: SiteQuality
SIO_000300: 9.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.311e0

ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.504709741490866e-5
allele num: 66458
num of homozygotes: 0

East Asian
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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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South Asian
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.02e-1

BaseQRankSum
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InbreedingCoeff
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FS
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QD
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MQRankSum
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VQSLOD
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DP
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MQ
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.3e-2

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

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66378
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South Asian
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allele frequency: 0.0e0
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African
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allele count: 15
allele frequency: 1.468285043069695e-3
allele num: 10216
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Latino
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allele frequency: 1.736111111111111e-4
allele num: 11520
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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FS
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SIO_000300: 1.878e0

InbreedingCoeff
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

Latino
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allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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South Asian
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
type: SiteQuality
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QD
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DP
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ClippingRankSum
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SIO_000300: 1.7e-2

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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GenotypeQuality
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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: 0.0e0
allele num: 16372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.522976721746472e-5
allele num: 66328
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.668616e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66326
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
type: Population
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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Other
type: Population
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Latino
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South Asian
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European (Non-Finnish)
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ClippingRankSum
type: SiteQuality
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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African
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allele frequency: 9.99000999000999e-5
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European (Non-Finnish)
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allele frequency: 4.557054320087495e-5
allele num: 65832
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South Asian
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Finnish)
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Other
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European (Non-Finnish)
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African
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East Asian
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Latino
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QD
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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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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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15732
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.528771479239283e-5
allele num: 65412
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.512257e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.505e0

VQSLOD
type: SiteQuality
SIO_000300: -8.628e-1

QD
type: SiteQuality
SIO_000300: 9.02e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 15544
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 8.210180623973727e-4
allele num: 8526
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65122
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

QD
type: SiteQuality
SIO_000300: 1.598e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

FS
type: SiteQuality
SIO_000300: 2.567e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.478831e6

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.45577792123951e-5
allele num: 15490
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64976
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.415e0

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.472155e6

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.233356857210068e-4
allele num: 8502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

DP
type: SiteQuality
SIO_000300: 1.468475e6

QD
type: SiteQuality
SIO_000300: 1.685e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

FS
type: SiteQuality
SIO_000300: 5.221e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546312045770837e-5
allele num: 64670
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.231e1

VQSLOD
type: SiteQuality
SIO_000300: -1.54e0

FS
type: SiteQuality
SIO_000300: 1.1426e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-1

DP
type: SiteQuality
SIO_000300: 1.465407e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.739219267560288e-5
allele num: 64606
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.805917576611483e-5
allele num: 11356
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.906e0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.46609e6

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.545117428924598e-5
allele num: 64720
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

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

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.547173314354674e-5
allele num: 64634
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
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
allele num: 10288
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64668
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 9.414422895876483e-5
allele num: 10622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 3.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

FS
type: SiteQuality
SIO_000300: 1.265e0

QD
type: SiteQuality
SIO_000300: 1.279e1

DP
type: SiteQuality
SIO_000300: 2.110462e6

GenotypeQuality
all individuals: 415
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 2.25e1
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: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545690614566588e-5
allele num: 64696
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.168e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.484e1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 6.026e1

DP
type: SiteQuality
SIO_000300: 2.112922e6

GenotypeQuality
all individuals: 2587
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6354
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.668534080298786e-4
allele num: 10710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64688
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

QD
type: SiteQuality
SIO_000300: 1.488e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

DP
type: SiteQuality
SIO_000300: 2.11341e6

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15955
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.825483753194597e-4
allele num: 10956
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.648e0

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

DP
type: SiteQuality
SIO_000300: 2.118029e6

FS
type: SiteQuality
SIO_000300: 4.434e0

QD
type: SiteQuality
SIO_000300: 6.64e0

VQSLOD
type: SiteQuality
SIO_000300: -1.066e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15949
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11870
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65054
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.42e-1

FS
type: SiteQuality
SIO_000300: 4.742e0

DP
type: SiteQuality
SIO_000300: 2.130721e6

QD
type: SiteQuality
SIO_000300: 1.088e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.255e0

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

GenotypeQuality
all individuals: 407
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 64
bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16581
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.607870242373975e-5
allele num: 65106
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.337502084375521e-5
allele num: 11994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 5.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

DP
type: SiteQuality
SIO_000300: 2.134004e6

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 1.257e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 275
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
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variant carriers: 0

GenotypeQuality
all individuals: 2938
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13330
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.499e1

DP
type: SiteQuality
SIO_000300: 2.148786e6

GenotypeQuality
all individuals: 1619
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14276
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518833535844471e-5
allele num: 65840
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.146e0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 2.772e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-1

DP
type: SiteQuality
SIO_000300: 2.16086e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.101e1

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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: 45
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.194e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.013e0

FS
type: SiteQuality
SIO_000300: 7.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.626e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

DP
type: SiteQuality
SIO_000300: 2.190673e6

QD
type: SiteQuality
SIO_000300: 1.552e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2003
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variant carriers: 0

GenotypeQuality
all individuals: 2965
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 3
bin: 1.75e1
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GenotypeQuality
all individuals: 6680
bin: 6.75e1
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 2.193404e6

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.401e0

QD
type: SiteQuality
SIO_000300: 1.442e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.84e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.193998e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

FS
type: SiteQuality
SIO_000300: 4.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.597e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.284e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.43427458617332e-4
allele num: 16432
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.201e0

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

FS
type: SiteQuality
SIO_000300: 8.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.15e-1

QD
type: SiteQuality
SIO_000300: 1.253e1

DP
type: SiteQuality
SIO_000300: 2.194957e6

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: 76

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

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

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

Latino
type: Population
allele count: 10
allele frequency: 8.637070305752289e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 37
allele frequency: 3.555640976359793e-3
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.051863857374392e-4
allele num: 66636
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.19834e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.766e0

QD
type: SiteQuality
SIO_000300: 1.335e1

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50220608097968e-5
allele num: 66634
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.01e-1

DP
type: SiteQuality
SIO_000300: 2.19387e6

VQSLOD
type: SiteQuality
SIO_000300: 3.67e-1

FS
type: SiteQuality
SIO_000300: 8.896000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.439e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

South Asian
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allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.364e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

InbreedingCoeff
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

South Asian
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allele count: 0
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VQSLOD
type: SiteQuality
SIO_000300: -1.694e0

DP
type: SiteQuality
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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SIO_000300: 5.898e1

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

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

Other
type: Population
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allele frequency: 0.0e0
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Latino
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East Asian
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European (Non-Finnish)
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allele num: 66654
num of homozygotes: 0

African
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South Asian
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MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4941
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 27
allele frequency: 2.332008982553118e-3
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

African
type: Population
allele count: 322
allele frequency: 3.095558546433378e-2
allele num: 10402
num of homozygotes: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.485e1

DP
type: SiteQuality
SIO_000300: 2.209791e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeQuality
all individuals: 4175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15741
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000300030003e-5
allele num: 66660
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.4039e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.188536e6

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.907e0

QD
type: SiteQuality
SIO_000300: 1.375e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

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

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

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

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.739e0

VQSLOD
type: SiteQuality
SIO_000300: 3.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 3.898e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: -9.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.188548e6

QD
type: SiteQuality
SIO_000300: 1.449e1

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

GenotypeQuality
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bin: 5.25e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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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: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2978
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.188576e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 1.549e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

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

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20763
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4960
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 4172
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variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 9.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

QD
type: SiteQuality
SIO_000300: 1.35e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 2.188526e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.697e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e0

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

GenotypeQuality
all individuals: 3285
bin: 9.25e1
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GenotypeQuality
all individuals: 4958
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.654e0

DP
type: SiteQuality
SIO_000300: 2.188419e6

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e0

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 1.832e0

QD
type: SiteQuality
SIO_000300: 1.443e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.124e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.137e0

QD
type: SiteQuality
SIO_000300: 2.004e1

FS
type: SiteQuality
SIO_000300: 6.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.188363e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.444000000000001e0

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

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

Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.035e0

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

Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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InbreedingCoeff
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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African
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European (Finnish)
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South Asian
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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DP
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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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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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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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Other
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South Asian
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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African
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Latino
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MQRankSum
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DP
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VQSLOD
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FS
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.3403499873193e-5
allele num: 15772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-3

DP
type: SiteQuality
SIO_000300: 2.172893e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.513042425709617e-5
allele num: 66092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.766e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.285e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.547930853850184e-5
allele num: 15272
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.159987e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.89e1

MQRankSum
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VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.356e1

BaseQRankSum
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SIO_000300: 3.22e0

ReadPosRankSum
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SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
all individuals: 1992
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14714
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 8.082000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.086e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.409e1

VQSLOD
type: SiteQuality
SIO_000300: -9.39e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 2.14738e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521282745611099e-5
allele num: 65734
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 2.140539e6

MQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.21e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

FS
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 8.008970046452026e-5
allele num: 12486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64948
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.100728e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.01667468334135e-5
allele num: 12474
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MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.100006e6

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.963864886095837e-4
allele num: 10184
num of homozygotes: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
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allele frequency: 8.107669855683477e-5
allele num: 12334
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64880
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.856100926473487e-5
allele num: 10146
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.374e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.089738e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.076e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549426712116517e-5
allele num: 64540
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

DP
type: SiteQuality
SIO_000300: 2.078792e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: 5.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.101352189554646e-5
allele num: 64488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 1.435e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.133e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.07168e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10070
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.553663538624075e-5
allele num: 64364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.465e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.798e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.055723e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.111871790882215e-5
allele num: 64270
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

QD
type: SiteQuality
SIO_000300: 1.252e1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

FS
type: SiteQuality
SIO_000300: 4.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.04584e6

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64270
num of homozygotes: 0

South Asian
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allele frequency: 9.167583425009168e-5
allele num: 10908
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10062
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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Other
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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